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CDX.
6.1.5 Reinstate a Cancelled Distributor Product
After entering the 'Basic Product Registration No' and 'Distributor Company Number' on the
'Application Info' screen, choose the 'Reinstate a Cancelled Distributor Product' option from the
'Application Type' dropdown.
The screen will darken and a spinning status wheel will appear. Once the system has finished
processing, a list of inactive Distributor Product Names will appear on screen. An additional
field will also appear on screen. The additional field is as follows:
• Application Name: The name of the application. You can change the name of the
application for easier identification. A default name will be generated by the system. This
field is required.
Text above the table will read: "Please select one or more inactive Distributor Product Name(s)
you would like to reinstate along with the Distributor Product:"
Exhibit 6-8 below displays the 'Reinstate a Cancelled Distributor Product' application type.
A
SSf Packages» Bafcii Uptoaih
Portal
- He*.


TEST ORG (Primary Submilei)
ft EP-4S111
Package lute
Package DocumeMs
* Applications)' 1
* OlitPio-OOOOOI-AII
Appfcaton Into
Appkca&on Documents
Application Info
Please Miter Ajipk-.iv/i Information n the ieMs below
Reguiatory Type CwtrbuVif Product
¦ Basle Product Registration 12^123
Ho



¦ Distribute* Company
Number
123



- Application Type
Rem«are * Canceled Dftfttutnr Product *



- Application Nam»
DatPto-OOOM 1 -ReSubnu
Pleat* select one or more inactive Distributor Product Namejs} you woKd like to
reinstate along wMi the Distributor Product
Distributor Product Name * Status e
El Weed Kin Phis Inactive
Weed Kjfer Extreme Inactive
Xtreme Rose and Flower Insect Kter II Inactive


Alter cntcwg UK reqiwed nfwmafcw,
selec! an epphea&nn type m 8>i?
'Appteaton Type' dtop down Once a type
is selected, a tot of Dustobutor Product
Nwics relieved torn Off wfl be
displayed Once the 1st e generated you
can iwtjss Itie "R««r button change the
Mark for Review



Hfisve Preview •/ Vakfale C Siihmi


CDX Inks -
Exhibit 6-8: Reinstate a Cancelled Distributor Product Application info Screen
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7
Batch Upload
The batch upload functionality of the PSP application allows you to upload packages created
using the e-Dossier Builder application or your company's IT systems in the XML e-Submission
format.
Important: Document file names within batch uploads cannot exceed 200 characters.
7.1 Upload Packages in the XML e-Submisslon Format
7.1.1
Home screen
To upload a package created using your company's IT systems in the XML e-Submission
format, click the 'Upload XML e-Submission Packages' link on the 'Home' screen.
Exhibit 7-1 below displays the 'Upload XML e-Submission Packages' option on the 'Home'
screen.
Pesticide Submission Portal
Pesticide Submission Portal
W10 the EPA'* Pes
Cuwenoy trio pwtat support! T»pes of tuttmnsjca PesotMe	ana tmia ftetpcme Tooeom a
Pesticide Submission
Data Call-in (OCI)
General Services
i
O
©
e
Create New Package
*o aetfe a new PSP package
Continue Saved Packages
Ta u6nttfce waiting on tMrt PS? pictiagrt
Package Status
Jo tsma; me *Ui'us or premoujiy ti
Upload XML e ^Submission Packages |
uptoJK) MrjOili flpt&atlOfH CI«IM
Upload e Dossier Builder Packages
To upload package* aeaa
i
Generate Root MRIDs
Exhibit 7-1: Selecting 'Upload XML e-Submission Packages' Option
Navigation: Click the 'Upload XML e-Submission Packages' link on the home screen.
7.1.2 Upload Packages Screen
Click the 'Browse...' button to upload a package created using your company's IT systems in
the XML e-Submission format.
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IMPORTANT: Please ensure that files within your package do not contain special characters.
Also, the XML within your package should have an e-PRISM prefix as the first part of the file
name.
After uploading the package, press the 'Submit' button to submit the package to OPP. You will
be navigated to the 'Create Passphrase' screen to create a passphrase that will encrypt your
uploaded package.
IMPORTANT: If you forget the passphrase, you will be unable to access the package. If you
lose or forget the passphrase, you must create a new package and passphrase. For security
reasons, the system administrator does not have access to the passphrase and will not be able to
retrieve it or reset it to a new one. To prevent losing access to submissions, OPP suggests that
each company agree upon and use the same passphrase for all submissions. A shared passphrase
also allows users within the same company to perform submissions for others if needed. If the
original creator of a submission (either completed or in draft) is unavailable for whatever reason,
the shared passphrase ensures that someone from the same company can retrieve and/or
complete the submission. OPP will be unable to retrieve or unlock the submission for the
company.
You will need this passphrase to access the copy of record for your batch upload. The
submission process will begin once you have created the passphrase. If you need assistance
creating a passphrase, please reference Section 5.2 above. If you need assistance with the
package submission process, please refer to Section 10. If your package does not pass validation,
you will have to make modifications to the package contents and XML and then resubmit via the
'Upload XML e-Submission Packages' option.
Exhibit 7-2 below displays a screen capture of the 'Upload XML e-Submission Packages'
screen.
Note: This screen will provide you a link to the correct page for uploading e-Dossier packages if
you mistakenly upload an e-Dossier package.
Balrh Uploadi * Ho*) *
TEST ORG (Pmrury Submflm)
Upload XML e-Submission Packages
cicstcd uw) your company's If sytteraii
COX Inks .
OPP Pesticide Submission Portal User Guide
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Exhibit 7-2: Navigate the Upload XML e-Submission Packages Screen
Navigation: Click the 'Browse...' button and upload a package created using your company's
IT systems in the XML e-Submission format. After the package is uploaded, click the 'Submit'
button to start the submission process.
7.2 Upload e-Dossier Builder Packages
7.2.1
Home Screen
To upload a package created using the e-Dossier Builder, click the 'Upload eDossier Builder
Packages' link on the 'Home' screen.
Exhibit 7-3 below displays the 'Upload eDossier Builder Packages' options on the 'Home'
screen.
H
PwtieWe Submission Portal
Pesticide Submission Portal
* Jo Uir EPA1* Pwaax Subraaton Porta*
CwrwitN ifto pots* supports fcvo C	PntKxte StadoaMon and Oala Caa-m R«pofr»e To M0n a tueratwn p«eaj£ VHeCl a f»pe tx
Pesticide Submission
Create New Package
I To OMle a ne*PS*> package
Data Call-in (DCI)
General Services
Generate Root MPIDs
To gencratr root WRI&»
Continue Saved Packages
To fenm* vwmrvj ©n t=Si> pstwges
©
e
To owck in* Matin of pmnuvs
pacMaei ana appirsflcev
Upload XML e-Submission Packages
to upload nawduai ap^cAfions creahrt
us*>9 >our tompanys it %yiMm
nipioa^BOossie^uilde^ackacje^
Exhibit 7-3: Selecting "Upload eDossier Builder Packages' Option
Navigation: Click the 'Upload eDossier Builder Packages' link on the 'Home' screen.
7.2.2 Upload eDossier Builder Packages Screen
Click the 'Browse...' button to upload a package created using the e-Dossier Builder. After
uploading the package, press the 'Submit' button.
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IMPORTANT: Please ensure that files within your package do not contain special characters.
Also, your package should contain a main.xml file, which eDossier Builder automatically creates
upon finalizing a package.
You will be navigated to the 'Create Passphrase' screen to create a passphrase that will encrypt
your uploaded package. You will need this passphrase to access your package.
IMPORTANT: If you forget the passphrase, you will be unable to access the package. If you
lose or forget the passphrase, you must create a new package and passphrase. For security
reasons, the system administrator does not have access to the passphrase and will not be able to
retrieve it or reset it to a new one. To prevent losing access to submissions, OPP suggests that
each company agree upon and use the same passphrase for all submissions. A shared passphrase
also allows users within the same company to perform submissions for others if needed. If the
original creator of a submission (either completed or in draft) is unavailable for whatever reason,
the shared passphrase ensures that someone from the same company can retrieve and/or
complete the submission. OPP will be unable to retrieve or unlock the submission for the
company.
If you need assistance creating a passphrase, please reference Section 5.2. Uploaded e-Dossier
Builder packages are converted into an online PSP form after being submitted. After creating a
passphrase for your package, all package data will populate onto the necessary PSP application
and you will be navigated to the 'Package Info' screen to name your package. You may then
proceed with package validation and submission as you would with a package created using the
PSP application. If you need assistance with package creation and submission, please reference
Section 5 and Section 10, respectively.
Note: This screen will provide you a link to the correct page for uploading packages created by
your company's IT systems in the XML e-Submission format if you mistakenly upload the
wrong package type.
Exhibit 7-4 below displays a screen capture of the 'Upload eDossier Builder Packages' screen.
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1 9
| Portal
asei • Batch Uptoads -
*
Its r OHG (Cnmary Suftirrftetl J
Upload eDossier Builder Packages
Please dctc the "Stows*" burton 1o upload lh« zip Sic era ated by #ic downloadable eDossmr Buidsr
fhe system vril convert <11o an oniric P5P package llvat you can modify, vaWale and submit
COXLnks-
Exhibit 7-4: Navigate the Upload e-Dossier Builder Packages Screen
Navigation: Click the 'Browse...' button and upload a package created using the e-Dossier
Builder application. After the package is uploaded, click the 'Submit' button. You will be
navigated to the 'Create Passphrase' screen.
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8 Continue Saved Packages
You can return to a saved package at any time via the 'Continue Saved Packages' screen. This
option is located on the 'Home' screen and within the 'Packages' dropdown in the application
header.
The 'Continue Saved Packages' screen allows you to view and access all packages with a status
of 'Awaiting User Completion.' All packages, which have not yet been submitted, will have this
status. You can create a new package from this screen by clicking the 'Create New Package'
button. You can also delete packages by clicking the 'Delete' icon in the 'Actions' column. To
access a package, click the blue link within the 'Package ID' column to navigate to the 'Enter
Passphrase' screen for that package.
Exhibit 8-1 below displays a screen capture of the 'Continue Saved Packages' screen.
TEST ORG (Pnmuy SubmflM)
Continue Saved Packages
To add a new package dek the "Ciif aDc New P.i-rkagr"
To ecM ,*n eximnfl pocknge tick aw Ink TncMoe 10*«
To defele ar> exiling package ctck ihe V icon m ttie lu
10 entile* found
Pickio* ID
Pacfcap* Nam*
Mocftflcaoon Oat»
Htms Per Pag*: ?5
Aetfon
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CDX.
Exhibit 8-2 below displays a screen capture of the 'Enter Passphrase' screen.
Enter Passphrase
Please enter your passphrase for the submission and click the "Next" button.
Or. you can click "Cancel" to return to the Home page.
Package Name EP-538
Enter Passphrase

| Cancel
| Next |
¦
A
Do Not Forgot Your Passphrase!
For security reasons, the system administrator does not have access to your passphrase and cannot retrieve it or reset it to a new one. If you have forgotten your
passphrase, you must create a new submission.
Exhibit 8-2: Enter Passphrase Screen
Navigation: Enter the passphrase that you originally created and associated with the package
and click the 'Next' button to navigate to the 'Package Info' screen, seen below in Exhibit 8-3.
Packages • Batch Uploads • Help *
¦TEST ORG (Pnmaiy Subtnflef)
ft EP-45117
[- Packiig* Into
Package Documents
Ckk frm Add Apple»4r/n iicilton and click
£»cJ) cegutaiofyrappfcafton tree to add
mem to your package After spw^mg the
number aaid types of apptea9rai* piois
8ie Save" buOon 1c save your dianges
fie ifls win .1 n?a astensk are tojubhJ
0
HiSavc APlnnrw r 'AiM Appfcjtari' button and cboaw *ie com pet-twill*)
Exhibit 8-3: Package Info Screen
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9 Validate
You can click the 'Validate' icon at any stage of completing a PSP package. The 'PSP Package
Validation' pop-up window is displayed when you click the 'Validate' icon. The 'PSP Package
Validation' pop-up window displays a report of all validation errors. During the validation
process, the application validates each screen of the PSP package to find missing and invalid
data.
Validation Errors: Errors can be fixed by clicking the error link. The links will display the
Screen Title Name (e.g., Package Info) and the associated error. After you click a link, the main
application screen will display the section where the error occurred so you can easily fix the
error. Once you have fixed the error, click the 'Validate' icon again to refresh the 'PSP Package'
pop-up window. If the information you fixed passes validation, the error will be removed from
the 'PSP Package Validation' pop-up window. You must fix all validation errors in order to
submit the package.
You can close the 'PSP Package Validation' pop-up window by clicking the 'X' button located
at the top right of the window.
Exhibit 9-1 below shows the screen capture for the 'PSP Package Validation' pop-up window:
PSP Package Validation:
•	Package Info
o Package Name is required.
•	Documents for the Package
o You have uploaded duplicated package level documents: ambiflufenamid Lab
Study.txt
•	DistPro-New-1: Application Info
o Parent Section 3 Number is required,
o Product/Risk Manager is required.
•	DistPro-New-1: Documents for the Application
o You have uploaded duplicated application level documents: Cover Letter.txt
Exhibit 9-1: PSP Package Validation Pop-Up Window
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10 Submit Package to EPA via CDX
Both Primary Submitters and Authorized Agents have the ability to sign and submit a PSP
package to EPA. Once you complete all required information and pass validation, the system will
allow you to submit.
10.1 Submitter Information Screen
Click the 'Submit' icon located in the application footer of the PSP application to access the
' Submitter Information' screen. The system requires you to review your contact information
provided during CDX registration and serves as a reminder for which company you are
submitting.
Exhibit 10-1 displays a screen capture of the 'Submitter Information' screen.
ft



Portal
IlHfcfi UpfcuKh • I (rip •

¦ IE SI ORG (ftnuiy Submits)
Submitter Information
Company Name
TEST ORG
Company Number
123
SubmitUr's Ro*t
Pnmary Submiatr
P»lt*
Mr
First Namt

MldoB* Initial
F
LastNam*

Phon* Numbtr
(333] 333-3333
Email Address

Mafling A
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CDXr
'X' icon and text on the screen will read: "Validation errors and/or viruses were found." A pop-
up window containing a list of validation errors will also appear. All validation errors must be
resolved before a package can be successfully submitted. For more information about validation,
refer to Section 9. If your package passes validation, the screen will display a green
'Checkmark' icon and text on the screen will read: "No validation errors were found. No viruses
were found."
Exhibit 10-2 below displays the screen capture for when no viruses or validation errors are
found.
iQp Packages - IWefl UptaHh ~ llelp-	TEST ORG ivnmary SubmMsr)
Submission Process: Validate
~
Vtfiji Scan service is not svatebte please try apa«i lattr
No vatdubun wror* bund
COXLriks -
Exhibit 10-2: Validation Passed
Navigation: Click the 'Continue' button to proceed to the 'Submission Process: PDF
Generation' screen.
10.3 Submission Process: PDF Generation Screen
Exhibit 10-3 below displays a screen capture of the 'Submission Process: PDF Generation'
screen.
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Sjf Packages* SafcliUploads. Help
Portal
TEST ORG (Primary SubnKter)
Submission Process: PDF Generation
COX Inks -
Exhibit 10-3: PDF Generation
Navigation: Click the 'View PDF' button to see a PDF representation of your package and its
contents. After viewing and/or printing the PDF, you can click the 'Continue' button to proceed
to the 'Cross-Media Electronic Reporting Regulation (CROMERR) Submission' screen.
10.4 Submission Process: 'Cross-Media Electronic Reporting Regulation (CROMERR)
Submission' Screen.
EPA's Cross-Media Electronic Reporting Rule (CROMERR) provides the legal framework for
electronic reporting under EPA's regulatory programs. CROMERR sets performance-based,
technology-neutral system standards and provides a streamlined, uniform process for Agency
review and approval of electronic reporting. The CROMERR program ensures the enforceability
of regulatory information collected electronically by EPA and EPA's state, tribal, and local
government partners.
On this screen you will enter your CDX credentials, answer a 20-5-1 question associated with
your CDX account, and certify your submission. For additional information about the 20-5-1
questions, please refer to the CDX PSP Registration User Guide. If your package is successfully
submitted, you will receive a 'Success' confirmation. You will also receive an email from the
CDX Help Desk once your package has been successfully transmitted to OPP.
Exhibit 10-4 below displays a screen capture of the 'CROMERR Submission' screen.
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A
o
Packages -
Batch Uploads -
He* - ifl
tisi c«o (Pnrwy Sut>m«er) 1
Portal



1
Cross-Media Electronic Reporting Regulation (CROMERR) Submission
Answer Se«et Quesaon
Certify
Uur 10
AWOREWTeST
Question
What k line first and mafcjto nwne ol your obml siting?
I cert^ under pen Jly ol l»w t)ia! Hat mfartnatori prcmied t\ tli» tfeicuitwnl a to
Sic best oJfflykn(y*rf«Sge and befef, Hue accurate and compiese I am aware
ttai Siere am $gmfcsist penalties Kt sufi-ninng false mtonnsten it-eiidngj the
possiiity of foes and nipflsonmen! for toMwnu wttetons
The	was sent to EPA The Copy of Record Ink to afcw tor $e
dnwntoad ol Vic Copy of Record and iigiMltite for fin vubnuswon ni appear n
the terms fe« when EPA receives and processes yow subroisson
ta>Xtnks .
Exhibit 10-4: CROMERR Screen
Navigation: After successfully submitting your package, click the 'Finish' button to proceed to
the 'Package Status' page, where you can view the details of submitted packages. Exhibit 10-5
below displays a sample package transmission email.
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Your PSP package (test) for THE DOW CHEMICAL CO. (123) has been
successfully transmitted to OPP.
Below are the application(s) included in this package and their tracking
number(s):
PreApp-New-000001: CDX_2015_000073
Company Name: THE DOW CHEMICAL CO.
Company Number: 123
If you have questions concerning this message, you may contact the CDX Help
Desk by email at helpdesk@epacdx.net or by calling the CDX Technical Support
Staff through our toll free telephone support on (888) 890-1995 between Monday
through Friday from 8:00 am to 6:00 pm EST/EDT. For International callers, the
CDX Help Desk can also be reached at (970) 494-5500.
CDX Homepage
https: //c dx. ep a. go v
United States Environmental Protection Agency - Central Data Exchange
Exhibit 10-5: Package Transmission Email
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11 Check Package Status and Download Copy of Record
The 'Package Status' screen allows you to check the status and details of your submitted
packages. You can check the tracking numbers of your applications on this screen, as well as
download a copy of record for your package. You can filter the packages on this screen by using
the 'Submission Type' and 'Submission Status' dropdowns. The status and submission date are
also shown. You will have to enter the passphrase used to encrypt the package, your CDX
password, and the answer to a 20-5-1 secret question to access the copy of record.
Refer to the 'Package Status Legend' within Exhibit 11-1 for the meanings of the different
statuses.
A




O
Poriol
Packages *
Batch Uploads •
He*j» J
^BrEST ORG (Prrnary Submflw)
Package Status
Below arc packages and appkcatons 3iat you have subtnfled
Ctck the Kxn n the 'ApfthatBtMsj' eokiiw» sh tfve iKing number^} ot the apptuaon^s)
Cfck 11 iv 'Copy of Rucotfl' icon n Bit table below to view Die package's copy ot tecofd
Padcag* Status L*garni
U\ Transmission: The package s m ijaismtsswst frwn PSP to OPP
Ponding: The package foas been transoiffleiS to OPP and & awasng processr^
Failad Transmission to OPP: Pie package failed tamaiitttm ta OPP
Partial Sucetss: Part o< JJte package was aueeeMluty etwisniKKd to OPP But we m more apjilcaliotti »itte package fa*w
Successfully Transmitted to OPP: Tr.e package was suecessluly transmce-d and processed by OPP
Milostont t Com pitted; Your packjg* Receipt Number ami Etatfronic Date SLPnp Itormctly Pin Punch Da'* I fmvc been
assigned and a contrrrjiBon email wl be sent
Submission Type: AIL
J tinlnti found
Picfcjg*ID *
BIM4907
BLM-4&21
EP-45T27
Submission Status ALL
Type
Butch
AppUcattonfa}
7©"
10
t0
Submission Oat»
01787016
01/28/2018
01(2*2018
Status
finding
Items Per Page: 25
Action(s|
0
Exhibit 11-1: Package Status Screen
Navigation: Clicking the 'Show Detail' button next to the application number will display the
tracking numbers associated with the applications in a submitted package. Clicking the 'Copy of
Record' button in the 'Actions' column will allow you to download a copy of record for your
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application. Click the 'Copy of Record' button to proceed to the 'Cross-Media Electronic
Reporting Regulation (CROMERR)' screen shown in Exhibit 11-2.
Cross-Media Electronic Reporting Regulation (CROMERR)
Please Enter Passphrase
Log in to CDX
Answer Secret Question
Package Name
test
Passphrase
User ID
ANDREW.TEST
Password
Question
What is the first and middle name of your oldest sibling?
Answer
sibling
Next I Cancel
Next I Cancel
Next Cancel
Exhibit 11-2: Navigate the CROMERR Screen
Navigation: Enter the correct data into the fields and click the 'Next' button to proceed to the
'Copy of Record' screen.
11.1 'Copy of Record' Screen
The 'Copy of Record' screen allows you to download a copy of record for your package as well
as download copies of files within your package. Click the 'Download Document' icon within
the 'Actions' column to download the requisite materials.
Exhibit 11-3 below displays a screen capture of the 'Copy of Record' screen.
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Copy of Record
1 d download a Copy ol Recwd, ckck on the grew anew under Vie Actors) cokwrin
File Harris
File Size
Application
Acdon(s)
CoRJESt OFtG_4512/.pdl
2044 KB
(POF)

0

tettSttl
Styles
i.i'ackaje Level)

©

tetfiw
9 bytes
PreA^NewUMOOOl COX JO 18 0020W

0


COX Links -
Exhibit 11-3: Copy of Record Screen
Navigation: Click the 'Download Document' icon within the 'Actions' column to download
copies of the materials within your package.
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12 Respond to DCIs
PSP allows users to see and respond to both GDCIs and PDCIs that OPP has assigned for
specific chemicals and products. Through PSP, users can review DCI information and submit
DCI Acknowledgements, 90-Day Responses, and Data Submissions. Users will also be able to
download a copy of record for their responses. Note: You will receive a notification email from
OPP when a DCI is awaiting your completion in PSP. To access your DCIs, click on the 'Data
Call-In' link on the PSP 'Home' screen. Upon clicking the link, you will be navigated to the
'DCI List' screen. Exhibit 12-1 below displays the 'Data Call-In' link on the PSP 'Home' page.
Pesticide Submission Portal
Pesticide Submission Portal
MMcomt to tho CPA* Petatid* 5
a portal aupjiom Two type* of submissions Pesbcrte Submasaxi and Data Cal m Response To b*gn it siibmisww please sekKl a
Pesticide Submission
Create New Package
to create a new PSP package
Data Call-In (DCI)
General Services
View stasus of Data CaWns
Sufim* responses to toe DCIs
Generate Root MRIDs
To tfenerale fcot MftlD*
lor study dot iWienis
Continue Saved Packages
ie wcking on PSP pactetg**
o
©
e
Package Status
To eiiiHk (he isatus of pfevOitsV vjbmmed
packages and apjibcaoorts
Upload XML e-Submission Packages
To uptoJKl Midmdualapptcatons ct&ated
us*i0 yoiif < ompany's IT iysicms
Upload ©Dossier Builder Packages
Exhibit 12-1: Data Call-In Link
Important: Document file names uploaded within the DCI section of PSP cannot exceed 200
characters.
Navigation: Click the 'Data Call-In' link on the PSP 'Home' screen.
12.1 DCI List Screen
The 'DCI List' screen allows you to see the details and statuses of DCIs that have been assigned
to your company. The type of DCI (PDCI or GDCI) is indicated as the first part of the ' DCI
Number.' You may go back to the 'Home' screen by clicking the 'Portal' link at the top left of
the screen. The list of DCIs can be sorted by the various columns. They may also be filtered
using the drop down filters available above the list. Once any portion of a DCI is submitted, a
'Show Detail' icon will appear next to the DCI number. This icon will reveal the tracking
numbers associated with the DCI. Please see the screenshot below for reference. Using the filters
and sorting feature will allow you to manage and customize your displayed list of DCIs. The
'DCI Acknowledgement,' '90-Day Response,' and 'Data Submission' columns can have any of
the statuses indicated in the 'Data Call-In & Response Legend.' These statuses indicate which
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point you are at within the DCI submission process. Exhibit 12-2 below displays the 'DCI List'
screen.
You mi»1 Jievif a Oat# (torn EPA ft? start a OCI Atkrwrteilge'neH To Start a OCI Ad kiwwtfdgBnjertt, tltth on Hie "Sun DCI
AcknonleitSiemeM' ink ri the coitespondria column
Alter Se DCI AtkiWHMtedgiwiicnt
Response" Ink m
to oPP; you may wart a £Q-Oay Response Please c&c* on fte "San so-Day
Sic- «4&3l80-0ay Response o succes-sfcity iransrftffled So adO prscessw) fay OPP. y
it "Su6m« Daw* m* « me cenespandeig eokfliw. v«i may submit iraiffipie mm »
You can ww s«d edit a DC! ArknomeJgeowmt SKM>ay Response at
a copy of record
i may start a Data SobmissEin f%ase ctck
itlTisfy nk reqturomenis
Qju Cill-m & Rf-ipon?* U*B»nd
Ho Action Available: No action s .ivaAs!>V tor Bus type ot response
Wo Action Reeded: TihiS a » legacy DCJ yog don't need W SutMftX DO A£|(Bdwt09tA>MI and livftal 5043ay U*iparf-*
Awaitipg User Completion: Th* Response » *i» «
0C1 AckneWtedgemint
e tS-Oaf Respome t
Data Subrolsston
GOCMOt101 -6657*151
11/20/2015
0?^&2018
Ptmttnj Jl
Ptndivj i
No Acton Avato&le
POCMgilBMSQ'9 0
11'i30>701&
02^awi5
Pnotfin^ i
Pendng £
Na Acson Avataaie
QOCHO11O1-1803Q
1t/20fi0t5
oa/za-wie
Pehift^J i
SuCCessfoSy TrafiSiaeed to OPP X
Pendatg
poa-ionet-tssft©
IIQOaOtS
02.7^7016
Pcnairg i
Ssiceessfutf Translated to OPP ±
fcrwling
GOCJ-101101.1W2Q
1tffl0r2015
(Qr2a.2016
Pentftig i.
Pendrig &
No Acton A«-ai»ble
P&CE-10110T-19I1 ©
"OOOOtS
02^2O1«
Ptni&ng 1
Succe«Ai»ir Transmitted to OPP 1
Pending
PDCI 111801-3JK178Q
0WI&OT14
01(03/2015
Perubrcg &,
Pe-ndng i
No Acton AvatoOie
60CI-J09600-1343 ©
0&26.9013
10.D4.2013
Pending Jt
Pending i
No A*>joj> AvatoDte
GOCI-2C®900-13hH 0
06/2&2013
10IW/2013
Pendstg £
PwWrnj i
NO Ac Son AvatoBle
Exhibit 12-2: DCI List Screen
Navigation: Review the DCI information on screen. If necessary, sort or filter the list of DCIs.
12.2 DCI Acknowledgement
The DCI acknowledgement is a simple form that allows you to confirm you have received the
DCI from OPP and will submit the requisite data. To begin a DCI Acknowledgement, click the
'Start DCI Acknowledgement' link in the list as seen in Exhibit 12-3 below.
After the DCI Acknow
90-Day Response" link in Hie correapoi
to OPP. you may start e SO-Oay Response Pleas* cl
it 90-Day Response is successfutiy transmitted to and processed by Of P. you may stan a Data
Pieese diet! an the 'Su&ma Date" link in the correspwiamg column You may ss*
satiety »s requironwrtt*
You C-Bn vie-.v orxt »dit a OCI Acknowledgement. 90-Day Response or Data
submitting, you may download a Copy Of record
before submitting After
Dele Cell-In A Response Legend
No Action Available: Nb action ss available tor ttws type of response
Awaiting User Completion: The Response Is In progress arvd has not boon submitted yet.
Failed Validation: The Response has validet-on error* end cannot be submitted.
In Transmission: Tne Response r* m transmission tram DCI to OPP
Pending: The package ftu &ee*t m»n*«wt« to OPP and t« awafQng processing
Failed Ti arremissiun to OPP; T»» Response failed UarnnniMiion to OPP
Successfully Transmitted to OPP: The Response --as suCcessfidy transmitted arxi processed by OPP
Start DCI Acknowledgement Submit an acknowledgement that you have received the Data Cafl-tn from EPA
Start 50-Day Response: Submit a X Day Response for the Data Call-In.
3ulMi«lt Data: Submit additional date to support your responses and satisfy guede&na*
Submit Data (Previous Submission Successful): Submit additional data Your fit
success?^ transmitted to OPP
ne: TEST ORO (123)
DCI Number: ALL
DCI Acknowledgement Status: ALL
OO-Day Response Status: ALL
DCI
QOCUIOI tOt-1972
PDCI-101101-1002
POCM11801-35059
OOCI-iOftMO-IM-l
Date t&sueo
il^Oi^OtS
U .'20.4015
09/18/2014
06,26/2013
02i^ft'2016
02/26-2016
OI >*03<2015
tO'04J2013
DC' Acknowtedgemoni
jstan PC-1
Start DCI Ac kne^ledifemenl
Stail DC-I Acknowledgement
Start DCI Acknowledgement
M0-Doy Response
No Action AveilaMe
ISfo Action AvedaWe.
No Action Available
NO Action Av®
-------
CDX.
Exhibit 12-3: Start DCI Acknowledgement Link
Navigation: Click the 'Start DCI Acknowledgement' link.
After clicking the link, you will be navigated to the 'DCI Acknowledgement' screen, seen in
Exhibit 12-4 below. You will see a list of DCI information displayed on screen, as well as two
checkboxes on the right side of the screen. Click the first checkbox to acknowledge receipt of the
DCI. The second checkbox is optional; it allows you to indicate whether you are an agent for the
specified company. After clicking the first checkbox, a blue 'Submit' button will appear on
screen. Click this ' Submit' button once you are ready to begin the submission process.
Note: The process of completing the DCI Acknowledgement form is the same for both GDCIs
and PDCIs.
Exhibit 12-4: DCI Acknowledgment Screen
Navigation: Click the first checkbox and the second checkbox (optional). Click the 'Submit'
button to begin the submission process.
After clicking 'Submit,' click 'OK' in the pop-up window that appears. The submission process
for DCIs is identical to the one for submitting PSP packages. Please refer to Section 10 for
assistance with the submission process. Once you have finished the submission process, you will
be navigated back to the 'DCI List' screen. The DCI Acknowledgement you submitted will have
a status of 'In Transmission' under the 'DCI Acknowledgement' column. There will also be a
green 'Copy of Record' icon next to the status. Important: You will not be able to start the 90-
Day Response until the DCI Acknowledgement status changes to 'Pending.' When the status of
the DCI Acknowledgement changes to 'Pending,' the 'Start 90-Day Response' link will appear
in the '90-Day Response' column. The timing of these status changes will vary. Exhibit 12-5
below demonstrates the 'DCI List' screen with the 'Pending' DCI Acknowledgement.
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1
You must have a Data Cat In trom EPA to tlart a DC' Acksiewfedgemeni To SI
Acinovyw-flQenienr mk m trie correspond*^ column
a DC> AcknomtedgemetW. c
y *tan a 90-Day Response Please ckck on iho "Slat CD-Day
After the CD Acfcnowteiigefnenl n tranvnoted to OPP you m
ei live coitesponaiiifl column
After tfw inmal SO-Qay Response is wiccessSglty transrrooed to ana processed by OPP you may start a Data Suamissson Pitas*
etc* on the "Submit 0st9"knk m the corresponds column You may subre* mmsie tmcs to sawfy af ie3 ±

Ho Acaoci Avatjfcie
PDCM01I01 1909G
11W2015
02/2*2010
Pending
1
PenOwtfl ±

No Acoon Avataoie
GOCI-1O11O1-19830
11000015
02/2912019
Pending
±
Su«es«IU^ transmitted to OPP
±
Pending
PDCt-101101 1810©
11000015
02f28.2018
Pending
A
Succession Tiat»vm«ed to OPP
i
Pendeig
tjOCM01101-1S8J 0
11000015
o20aooie
Pending
4
Pendng ±

No Ac Bon Avatoble
PDCM01101-1611 S
1100/2015
02*28/2016
Pending
±
Successful Transmitted to OPP
±
Pending
GocMonoi-iewQ
11000015
02030016
] Ponding
M
1 	1

No Acbcn Ava toWe
POCMQ110M9981
11000015
02*28/2016
Start DCI Acknoy
rfedgemen!
No Action Available

No ActHn A'lafotile
POO-111801 350760
09-15.2014
01/03/2015
Pending
X
Pending A

No Action Avafatile
GCCI-30960G-1343 0
06080013
tO-04.2013
Pending
±
Pendog i.

No Ac ocn AuataS'Kt
GOCI-2Q9600-t3*1 0
06-26-2013
10/040013
Pending
±
Pentfwg i.

No Ac Bon Avatitile
COX I nks -
Exhibit 12-5: 'Pending' DCI Acknowledgement
You will also receive a notification email from the CDX Help Desk indicating that your DCI
Acknowledgement was successfully transmitted to OPP as seen in Exhibit 12-6 below.
Your DCI Acknowledgement of Receipt (GDCI-101101-1972) has been successfully transmitted to OPP
and is awaiting processing. Your tracking number is CDXDCI 2016 000001.
Your 90-Day Response is now open and you can start the submission.
Company Name: TEST ORG
Company Number: 123
If you have questions concerning this message, you may contact the CDX Help Desk by email at
helpdesk@epacdx.net or by calling the CDX Technical Support Staff through our toll free telephone
support on (888) 890-1995 between Monday through Friday from 8:00 am to 6:00 pm EST/EDT. For
International callers, the CDX Help Desk can also be reached at (970) 494-5500.
CDX Homepage
https://cdx.epa.gov
United States Environmental Protection Agency - Central Data Exchange
Exhibit 12-6: DCI Acknowledgement Email
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12.3	90-Day Response
The 90-Day Response allows you to review and respond to studies/guidelines as outlined in the
DCI. After indicating whether or not you will satisfy the DCI data requirements, you will get the
opportunity to respond to each guideline and provide additional documents/data as necessary.
The following sections detail 90-Day Responses for both PDCIs and GDCIs. To start a 90-Day
Response, click the 'Start 90-Day Response' link under the '90-Day Response' column as seen
in Exhibit 12-5 above. You will have to create a passphrase for your 90-Day Response; please
refer to Section 5.2 for assistance with creating a passphrase.
IMPORTANT: If you forget the passphrase to your DCI, you will be unable to access it. For
security reasons, the system administrator does not have access to the passphrase and will not be
able to retrieve it or reset it to a new one. To prevent losing access to submissions, OPP suggests
that each company agree upon and use the same passphrase for all submissions. A shared
passphrase also allows users within the same company to perform submissions for others if
needed. If the original creator of a submission (either completed or in draft) is unavailable for
whatever reason, the shared passphrase ensures that someone from the same company can
retrieve and/or complete the submission. OPP will be unable to retrieve or unlock the submission
for the company. The same passphrase must be used throughout the life of the DCI.
12.4	GDCI 90-Day Response
The following sections detail the process of completing and submitting a GDCI 90-Day
Response. GDCIs may contain multiple EPA Registration Numbers. Unlike PDCIs, GDCIs
contain a single list of guidelines regardless of the number of EPA Registration Numbers. If you
choose to cancel or claim a generic data exemption for ALL EPA Registration Numbers, you
will not have to respond to any associated guidelines. Otherwise, any guideline responses you
indicate will be applied to all the EPA Registration Numbers for which you have agreed to
satisfy data requirements. Please refer to the subsequent GDCI sections for more details.
IMPORTANT: If you forget the passphrase to your DCI, you will be unable to access it. For
security reasons, the system administrator does not have access to the passphrase and will not be
able to retrieve it or reset it to a new one. To prevent losing access to submissions, OPP suggests
that each company agree upon and use the same passphrase for all submissions. A shared
passphrase also allows users within the same company to perform submissions for others if
needed. If the original creator of a submission (either completed or in draft) is unavailable for
whatever reason, the shared passphrase ensures that someone from the same company can
retrieve and/or complete the submission. OPP will be unable to retrieve or unlock the submission
for the company. The same passphrase must be used throughout the life of the DCI.
12.4.1 GDCI 90-Day Response Submission Screen
After clicking the 'Start 90-Day Response' link, you will be navigated to the '90-Day Response
Submission' screen. This screen contains summary information about the DCI. You can also
upload DCI-level documents on this screen. A navigation tree is also present, pictured below in
Exhibit 12-7.
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Exhibit 12-7: GDCI Navigation Tree
The following fields are displayed on the '90-Day Response Submission' screen:
•	Company Name: The name of the company for which the DCI was issued. This field is not
editable.
•	Company Address: The address of the company for which the DCI was issued. This field is
not editable.
•	DCI Number: The DCI number. This field is not editable.
•	DCI Type: Indicates whether the DCI is a GDCI or PDCI. This field is not editable.
•	Issued Date: The date the DCI was issued. This field is not editable.
•	90-Day Deadline: The 90-Day deadline of the DCI. This field is not editable.
•	CRM: The Chemical Review Manager. This field is not editable.
•	Chemical Name: The name of the chemical associated with the DCI. This field is not
editable.
•	Chemical Number: The number of the chemical associated with the DCI. This field is not
editable.
The 'Summary of the DCI' table on the right side of the screen displays the EPA Product
Registration Numbers and Guideline Requirement Numbers associated with the DCI.
The document upload section contains the following document types:
•	Correspondence
o Submission Cover Letter
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Study
o Voluntary Cancellation / Use Deletion
o Time Extension Request
o Transmittal Document
Please note: If you upload any study documents, you must have a corresponding Transmittal
Document uploaded at the DCI level. If you upload studies in subsequent data submissions,
you must have a new transmittal document for each of those data submissions.
Exhibit 12-8 displays the '90-Day Response Submission' screen.
A OCI MumS*c
oocMottet-mi
* . 90 0*. «wee«w sutwreson
k EPA «eg Hs W2-5M
EPA Rug No 353-388
- EflAflefl NO S42-V9I
' R»qulr»m«rt SUUI A
RitpeiiM
Acute OMinit urMftwn •
87015C0
ifllfce AM OCI
O
riwt«(ire JtPAPic
EPA Product R»g ii
Sumnauy or th* DCI (OOCMfl lto1-HTt)
utr ReflBiiaucn .Number n i mi J ciuw
ui p*J4o m»e Mil* aial y®u iwpooa io eacn o< »r *01101

Documtnt Tjrp# CTKWSe
Docunwnt SuBt|rp» tMathf.
Exhibit 12-8: GDCI 90-Day Response Submission Screen
Review all di splayed information and upload DCI level documents if necessary. To upload
documents, click the 'Add DCI Level Document' button. After clicking the button, choose a
'Document Type' and 'Document Subtype' and upload files by clicking the 'Browse...'
button. You may also enter comments if desired. After selecting a document for upload, click
the 'Save' button. Any uploaded documents will display in the documents table in the center of
the screen. You may remove any uploaded documents by clicking the red 'Delete' icon in the
'Action(s)' column. Refer to Exhibit 12-9 below.
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S i no-ila-i cut renin lou(« ¦
6701103
9CKJa> ueitnat ttoKiti ¦
CT03JSO
AddflKmal Etna* Ratiptonts
Somnury a* OM OCI lOOCMOt t0t-l*T2)
DCi Typ> Ornenc
IMUM Dlti 'v;'.! V".
M-Cji DvJOIll'-* 02 25-20"5
crA Product Rvgntratiion N
CNmHtat Nu«««t to 1101
FO> Typa
Ct*le»panOe*e
Secmwon Cma Lefier
Exhibit 12-9: Navigate the GDCI 90-Day Response Submission Screen
Navigation: Review the displayed information and upload DCI level documents if desired. Click
the 'Next' button.
Note: For information about the 'Save,' 'Preview,' 'Validate,' and 'Submit' buttons in the
application footer, proceed to Section 5.4. Otherwise, proceed to the next section.
12.4.2 GDCI EPA Product Registration Screen
This screen contains basic information about an EPA Registration Number. On this screen, you
may choose one of three radio button options. Select a radio button option for each EPA
Registration Number (if more than one) before proceeding to the 'Requirement Status &
Registrant Response' section.
The following information is displayed on the 'EPA Product Registration' screen:
•	EPA Registration Number: The EPA Registration Number associated with the DCI. This
field is not editable.
•	Product Name: The Name of the product associated with the DCI. This field is not editable.
The following radio button options are available:
•	I wish to cancel this product registration voluntarily: Selecting this option will cause a
file upload section to appear.
Exhibit 12-10 below demonstrates this selection. A document must be uploaded to support
the cancellation. Click the 'Add Document' button, choose a 'Document Type' and
'Subtype,' and upload a document via the 'Browse...' button. Any uploaded documents will
appear in the documents table in the center of the screen. You can delete added documents by
clicking the red 'Delete' icon in the 'Action(s)' column. The document types are as follows:
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ft DC! Kwnvo^f
coa-ifriievitra
* 90- L-n teipttue Sutw-wucr.
I . CPA Wcy NO SflJ-SM
EPAUeq Ho 352-888
EPA Hi
J 3M-M
Rwuiwnrm «3CU1 A
ftvgiitnnrs R»s-ponv»
21>2«-0ayo.
670 3300
o Correspondence
¦	Company Letter
¦	General Correspondences
EPA Product Registration (EPA Reg. No. 352-596)
EPA Registration Mumfc»r
ITodu-ct N»m«
etttiis prooucl regtHraJKyi veauntjfa, I
l am clMrmg J Genet* OM ExefrpSioo t^c jwm I otXan She atWe
i agroe to sans?r Oener* Data »wpjtne#nenw w «k*4wj on u* ati»
me source EPA teyrMialcn mitnter toSed Drtow
Rjfm emtiM-n upioad
r
EPA Product Registration (EPA Reg. No. 352-596)
Plc«ti»r tcfc-.l lit*	wptkm takm Only wi
EPA R.ui»tr*U«r> Hum bar	JS2-54S
Product Nam*	DUPONT CANOPV SP MERBICIDe
1 Vaoti M itaiu«l Ihoi product rcgftlftMn MlunlAn^
< agree lo Ml&ty Oexieic Data it
<1 "Requiermnts SUflus diKl Reg&mnf s Restiwise "
S«ure» EPA R*oinrmion
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blue 'Add Another Source EPA Registration Number' link. You may delete any added
numbers by clicking the red 'Delete' icon next to the text box. After you have finished
adding numbers, click the 'Next' button.
Exhibit 12-11: GDCI Generic Data Exemption
Note: All entered Source EPA Registration Numbers will be validated during submission or
when you press the 'Validate' button in the Application Footer.
Navigation: Enter all required 'Source EPA Registration Numbers' and click the 'Next' button
to respond to the other registration numbers (if any).
• I agree to satisfy Generic Data requirements as indicated on the attached form entitled
"Requirements Status and Registrant's Response": Selecting this option requires no
additional data. Exhibit 12-12 below demonstrates this selection. After selecting this option,
click the 'Next' button; you can continue navigating through the DCI.
i DCINumiMf
ODCMI1101-197 2
SO-Dsy Response Submission
I- EPA Reg No 362 -566
I EPAIteg No 362-888
EPA Reg No 362-MI
R«qu
2t0&dnv de«mal tenacity
870)200
yO-iJay dermal tonicity •
•70 3250
Em*! Reciptwil*
Select *ie «ppf«irs»te opaon.
uippontm dw.unviMavifl d n«£i!4«« ause I n4itam the a< we ngredicnt from the source EPA reostraacn number tiled betaw
! agree to safety Generic Data requirements. its «'J« a$ed on the attached term
Status ar-d Registrant's Response "
Exhibit 12-12: GDCI Agree to Satisfy Data Requirements
Navigation: After selecting this option, click the 'Next' button to respond to the other
registration numbers (if any).
Note: If an option has been selected for all EPA Registration Numbers, click the 'Next' button to
proceed to the 'Requirement Status & Registrant's Response' section (Section 12.4.3),
Important: Your responses to the guidelines in the 'Requirement Status & Registrant's
Response' section will only apply to the EPA Registration Numbers for which you agreed to
satisfy the Generic Data requirements (third radio button). If you select the first or second radio
button for ALL EPA Product Registration Numbers, you will not have to fill out responses for
OPP Pesticide Submission Portal User Guide
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any of the guidelines. In this case, a gray strikethrough line will appear in the navigation tree and
red text will appear on the guideline pages. See Exhibit 12-13 below for reference.
ft DCI Number
GDCI-101101 -1972
i 90-Day Response SUamisstcn
I I- EPA Reg. No. 352-596
j U EPA Reg. No. 352-888
| L EPA Reg. No. 352-991
i- Requirement Status &
Registrant's Response
870.3250
Additional Emar. Recipients
Select a response from tfw 'Registrant's
Response drop down. Select a document
type and upload a supporting document If
applicable. You may enter any additional
;nformalion into the 'Comments' text box.
O
Requirements Status and Registrant's Response (Guideline No. 870.2500)
You dont need to fill out this form because you either canceled the product registration(s) or claimed generic data exemption(s) for all EPA Product Registration Numbers.
You can skip reviewing the guidelines by clicking the 'Additional Contact" button to add more email recipients, or the 'Submit* button to start the submission process.
GuldeLine Number	870.2500
Study Title	Acute dermal irritation
Target Submission Date	07/20/2015
Protocol	N
Use Pattern	D: R; AA DD
Test Substance	EP: MP: TGAI
Time Frame (month}	8
* Registrant Response Please select a Registrant Respon
Comments
Legend and Footnote (Guideline No. 870.2500}
Use Pattern
D - Aquatic food crop
R - Agricultural premises and equipment
AA - Antitoullng coatings
DD - Aquatic areas
Test Substance
EP; MP; TQAI - End Use Product; Manufacturing Use Product
Technical Grade Active Ingredient
Footnote; s)
3. Not required if test material s corrosive to skin or nas a pH of less
lhan 2 or greater than 11.5.
5. Not required if test material is a gas or a hlghsy volatile liquid.
Hsave OPreview ~Validate 0 Submit
Exhibit 12-13: GDCI Response to Guidelines Not Needed
Navigation: Since no guidelines require a response, you may click the 'Additional Contact'
button to specify additional email recipients for DCI email updates, or the 'Submit' button to
begin the submission process.
12.4.3 GDCI Requirements Status and Registrant's Response Screen
This screen contains information about a Guideline Number within the DCI. On this screen, you
may choose a response from the 'Registrant Response' dropdown. After selecting a response,
additional fields or a document upload section may appear so that you can submit data to support
your response. You may also enter comments about the response into the 'Comments' text box.
You must respond to all guidelines before submitting the 90-Day Response.
The following information is displayed on the 'Requirements Status and Registrant's Response'
screen:
•	GuideLine Number: The Guideline Number associated with the DCI. This field is not
editable.
•	Study Title: The study associated with the guideline. This field is not editable.
•	Target Submission Date: The targeted date for submission. This field is not editable.
•	Protocol: The protocol for the guideline. This field is not editable.
•	Use Pattern: The use pattern for the guideline. This field is not editable.
•	Test Substance: The test substance for the guideline. This field is not editable.
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• Time Frame (month): The time frame for the guideline. This field is not editable.
You may select a response for the guideline via the 'Registrant Response' drop down. You can
also copy a response to all guidelines within a DCI by clicking the blue icon next to the
'Registrant Response' drop down and clicking 'OK' in the pop-up window. This will ensure that
all guidelines have the selected response applied to them. You can later change the response for
the affected guidelines if you wish. See Exhibit 12-14 below
A DCI Numf»r
GDCMG110t-1972
S4-Day Response SutomttMin
EPA Reg, No 343-SW
EPAiteo Ho 352'688
EPA flea Mo 3SJ-9&1
R«qu»r«rn#rt Statu* i
RifllJVJM'i Rtlpcmi*
. Acute mta&ort -
070.2500
2 iQauay detroai toxcty
670 3200
90-day demnfll uuktf
8703250
Err>alRp' bo*
H Save ttrVevew ~Vw befcsv
GuKltfLwie Number 670 7500
Study Tid» Acute dermal utiaton
Targai 1
Tast
Q7tf0/20t6
U» Patwm	0. R:. AA DO
I	EP MP TGAI
Tlma Pramt ?uicalGrade
Aetata Ingredient
Foo
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CDX.
Select the 'Correspondence' document type and the 'General Correspondences' subtype.
Enter any comments if necessary. Upload a document via the 'Browse...' button. Click the
'Save' button. The uploaded document will appear in the documents table in the center of the
screen. You may delete an uploaded document by clicking the red 'Delete' icon in the
' Action(s)' column. After uploading a document, you will not be able to change your
'Registrant Response' selection. You will have to delete all uploaded documents before you
can change your response. See Exhibit 12-15 below.
ft OC» Number
QDGH01101-1972
•*- 9©-Oay Response Submission
CPA Reg No 352-596
EPA Beg No 352 -838
£PA Reg No 352.001
Requirement Status ft
RtflM(rant's Respoos*
Acute dermal ertaton •
870 2M0
J 173-day irrmal U>»c8y -
8703200
90-day dermal -
6703250
s'drop down Select* document
and uctoad a supporting dorume nt H
flppVabie Vo*j may enter any addfconal
etiofmetiian nto the 'Commarvt*' text bo*
M Save mpmnem ~ VnMate CjSubm*
um Pattern	0D: AA: R, D
T«$t Subsume	EP. MP TGAI
time Pram* (month)	3
¦ Registrant Response AjJWerrmnr to GW S'lair-
j
EP MP TQA) ErmtoeProduci M^rsuiacium^ Use Prortuci Terhnieiit Grade
A£5ve Ingredient
FMHMtli]
3 Not requted It test matenal a corrosive Jo sJun or has a pH of less ihsn ? or
greater than 11 5
5 Not requns) if tev material is a ga«
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CDX.
A DGINumlier
GDCMOI tOt-1072
| BO-Day Re-vporvw
f- i EPA Reg No 352-5*6
| CPA Reg Mo 362486
gPAKeg No 3W-891
* R«quirtfD*m Sunji ft
Registrant's Response
| - Acute dermal irrtMon -
870 2500
I , ?1/2S-daiy dcrnuil tone*?
8703200
99-day dermal toxict/ -
870.3250
1 A#ti#>onai Emu' Ret
Select a response from the 'Registrant's
Response' drop dowv Selett a document
lype and upload j suppwtmg document if
jppkjWe Ytwj may entei any add&Gnaf
n mo Vie "Comments text Dc»
HSure a Preview •/ VaMsie C SwBmi
Protocol
Use Pattern	DO AA R D
Test Substance	TGAI
Time Pram* (month)	24
¦ Registrant Rtspc-ns*	Agreement to Ccr,: Share
CMIfflllHl
0 • Aijualr. lood ciap
Tttt Substance
T GAJ - Technic al Grade Ac */t Ingredient (IGAJj
Footnote(s)
2 Reqived to a^ncuSural uses repeated iturt
occui Not required (fan at ceptabte 90/fay derma
4 £P tmstmg a required a eie product or any component ol t roary ncrease
deimaf absarpoon of the active ngred«wit(s) as de*erm«ed by leslng usirvg me
TGAI of ncreast? tgar oi pharmacologic efiecte
k> N«w Document
Use Previously Uploaded Document I
¦ Uploaded Documents Test2 Wl
Document Typ*	Correspondence
Document Subtyp»	General Correspondences
Uploaded FKe	Tn-vC a!
Exhibit 12-16: Reuse Document Option
Exhibit 12-17: Reused Document in the Documents Table
Navigation: Click the 'Use Previously Uploaded Document' radio button. If any documents
are available for reuse, select the appropriate document from the 'Uploaded Documents' drop
down. If no documents are available for reuse, you will get an appropriate message. Click the
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'Reuse' button and click 'Next' if you are finished uploading documents to the response.
Clicking 'Next' will navigate you to the next guideline in the DCI.
•	Offer to Cost Share: This response requires at least one 'General Correspondence' and one
'Form 8570-32 (Certification of Attempt to Enter into an Agreement with other Registrants
for Development of Data)' document upload. This response has the same document types as
'Agreement to Cost Share.' Upload the necessary documents and click the 'Next' button to
proceed to the next guideline.
•	Submitting Existing Data: This response allows you to upload study documents. It features
the standard file upload feature, but also allows you to enter an MRID for your study via the
'MRID' field. For assistance with generating a root MRID, please refer to Section 4. The
document types are as follows:
o
Study
Data Entry Spreadsheet Template (DEST)
Data Waiver Request
Protocol
Study
Study Profile
Supplemental Study Data
Transmittal Document
Water Monitoring Data
Upload all necessary documents and click the 'Next' button to proceed to the next guideline.
See Exhibit 12-18.
Note: The MRIDs you enter will be validated during submission or when you press the
'Validate' button within the application footer.
A PCJNum&tf
eoei-101101-1972
* 9D-Qiiy FtoapcriM SubmiMUan
I fcPA*»g Ne 362-Stt
1 EPA Flog NO 352-aaa
EPA No S52-891
8*gi9ir*nrs ftespons-#
Acute djpriri ifraeon •
#702500
21 f2W«y Wtrn#i	-
070 3200
9CWJoy	Wile By -
•703260
AtMBIonal
a r*rspcn»e flcm tft« tlagWrsnf *
RctponM1 area down 2et»ti a document
o «w>« owi ooa>»c
Add New Document
&>' 1M ifai r&jie sm a mta&ois* it !h* mm
itctafy
1. CP 5883ns A	.rf Pi# BffidLftt Of Wry eOff«OWK S!
¦n»y Increase dermal otoscspltoci of tn» ac".'« lr
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CDX.
Navigation: Upload all necessary documents, enter MRIDs, and click the 'Next' button to
proceed to the next guideline.
•	Upgrading a Study: This response allows you to upload study documents. It features the
standard file upload feature, but also allows you to enter an MRID for your study via the
'MR1D' field. For assistance with generating a root MRID, please refer to Section 4. This
response has the same document types and features as the 'Submitting Existing Data'
response.
•	Citing a Study: This response allows you to cite studies. It features an 'MRID Number' field
so that you may enter the MRID of the studies you are citing. You can click the 'Cite an
additional MRID Number' link to cite multiple studies. You can also delete MRIDs by
clicking the red 'Delete' icon next to the 'MRID Number.' See Exhibit 12-19 below.
A DCI Number
GDCM 01101-1972
¦» 90-D«ry Response Sutxnlssion
EPA Reg. No. 352-596
EPA Reg. No. 352-888
EPA Reg. No. 352*991
» Requirement Status &
Registrant's Response
Acute dermal irntation •
870.2300
21,"28-day dermal toxicity -
870.3200
90-day demtal toxicity -
870.3250
Additional Ema» Recipients
Select a response from the Registrants
Response' drop dawn. Seiect a document
type and upload a supporting document if
applicable. You may enter any additional
Information into the Comments' text bo*.
H Save Q Preview ~Vai
Study Title	90-day dermal toxicity
Target Submission Date	11 ^2017
Protocol	N
Use Pattern	DO: AA R, D
Test Substance	EP: TGAI
Time Frame (month)	24
- Registrant Response	Citing a Study
Comments
MRID Number	123-55678
MRID Number	87654321
MRID Number	11223344
4* Cite an ad«fitwr*al MRID Number
Use Pattern
OD • Aquatic areas
AA - ArttitouSng coatings
R - Agricultural premises and equipment
O - Aquatic food crop
Test Substance
EP TGAI - End Us
i Product: Technical Grade Active IngretSen?
Footmote(s)
t Required for food uses If either of the foifcwlng criteria is met
(I) the use pattern is such that tne dermal route 'would be tne
primary route or exposure: or (It) tne active Ingredient is known or
expected to be metabolized differently by the dernial route of
exposure than by the oral route, and a metabolite is the toxic
moiety
4 EP testing Is required if the product or any component of It.
may increase aennal absorption of the active ingredients i as
fletermined by testing using the TGAI, or increase toxic of
Exhibit 12-19: Citing a Study
Navigation: Enter the necessary MRIDs and click the 'Next' button to proceed to the next
guideline.
•	Deleting Uses: This response features the same file upload feature found in other responses.
The document type and subtype are as follows:
o Label
¦ Draft
Upload the necessary documents and click the 'Next' button to proceed to the next guideline.
•	Low Volume/Minor Use Waiver Request: This response features the same file upload
feature found in other responses. The document type and subtype are as follows:
o Correspondence
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¦ Waiver Request
Upload the necessary documents and click the 'Next' button to proceed to the next guideline.
• Waiver Request: This response features the same file upload feature found in other
responses. The document type and subtype is the same as the 'Low Volume/Minor Use
Waiver Request' response. Upload the necessary documents and click the 'Next' button to
proceed to the next guideline.
12.4.4 Additional Email Recipients and GDCI Submission Process
After all guidelines have been responded to, you may indicate additional email recipients on the
'Additional Email Recipients' screen. This screen allows you to indicate additional email
addresses to which DCI notification emails will be sent. By default, these emails are only sent to
the PSP account that performs the submissions. These emails will inform the recipients when 90-
Day Responses and Data Submissions are submitted to OPP.
Click the 'Add a new email address' link. An 'Email Address' text field will appear. Enter the
email address of the desired recipient. If you would like to add more than one email address,
click the Add a new email address' link as many times as necessary. You can use the red 'x'
icon in order to delete entered addresses.
Once you are finished entering email addresses, click the 'Submit' button to begin the
submission process. Press 'OK' in the pop-up that appears. See Exhibit 12-20 below.
A DCI Number
GDCI-101101-1972
*	90-Day Response Submission
EPA Reg. No 352*556
l- EPA «eg Mo. 352-S8®
EPA Reg. No. 352-991
*	Requirement Status &
Registrant's Response
AcuM dermal Irritation -
670.2500
21 i28-day dermal toxicity *
870.3200
90-day dermal loxlctty •
870.3250
Additional Email Recipients
Emer one or more emaii addresses If you
v.1*h to specify more than one email address,
please click the plus "•*" sign and enter the
i. The *pocifi»d email »ddros*«*
e updates on Pw DCI's status
O
H Save fil Preview ~Validate CJ Submit
Additional Email Recipients
Please enter one or more email addresses below.
If you wish to specify more than one ernast address, p-sease tuck the plus V sign and enter the information. The specified a
ill addresses also receive updates en the OCrs status
Email Address
obc'S-gmall.com
Email Address
t23-JSvahoo.com
a
+ Add a new email address
Exhibit 12-20: Additional Email Recipients
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Please refer to Section 10 for assistance with the submission process. After you have
successfully submitted the DCI, you will be navigated back to the 'DCI List' screen. Your
submitted DCI will have a status of 'In Transmission.'
Important: You will be able to submit data once your DCI '90-Day Response' status changes to
'Successfully Transmitted to OPP.' See Exhibit 12-21 below.

OCHst
Heto *
a i
11 ccrrtspQntmg column
After th« 0C3 Ac Knc wtertgenwrvl a transmitted to OPP you may start a 90-0ay fiesc-crvse Pk-aic tick on the "Star: 90-Day
Response" ink n Uve coriespoodrng column
After Hie intual 90-Cay Response is sutces»«u% fransmeed to and processed Cry Of*" you ma* sw/t a Data Subtntssjon Please
cfccfc on the "Submit Data" Ink in V>» cofratspofldng column You may submt mufcpte snn to satisfy al nrijiiirerr*r>t»
You t an view and edit a OCI Acknowledgement 90-Day ftespor.ie or Data Submtewon before submntng After submffing. you may
No Action Available: No neson k available- Itw tTii* cl response
No Action	Tha 14 0 teflacy DCI you fltonl need to suftmit DCI Aeknov*ted8«it>ent and irsfcai «HJay Response
Awaiting l>s»r Completion; rjio Response ts m progrcv- anotias norbcers suftmfWd ye«
Failed Validation: The Response »ias vatdaton triors and >camno< be su4>mffleij
in Transmission: rn« Response a *1 i/anstnwsloo from DClto Off
Pending: The pdOuige fidri been transmitted to OPP and is awoftng processing
Failtd Tran«m 15 Hon to OPP: I he* Response tolled Vanvnrvsion to OPP
SireeessMly Transmitted to OPP: The Response was successfully transmitted and processed by OPP
Start OCI Aek nowledgemenc Submit an ac knowtodgemenf that you have raceneu 0i« Data Cal-ln from EPA
Start 90-Day Response Sufom* a 90-Day Response tor the Data Cal-ln
Submit Data. Sue me aiftinoival data 10 support your iesponse* and sowfy guaSeknes
Submit Data (Previous Submission Successful): Subii*4 additional data four pteinous submission was successful
a to OPP
iy Nam. TEST ORG (123)
OCI Number: ALL
OCI Acknowledgement Status: ALL
90-Day Response Status: ALL
Items Per Page: 25
OCI Number
ODCMOItOI-89678 Q
PDCM01»01-1B09©
OOCMOUD1-t9ft3©
gocmqi 101-1 see 0
PDCMQ11O1-191O0
GOCMO1101-1982 0
POCM01tO1-19110
POCM0t10M9&81
poci-11 ioousots o
ODCI-2M®QO-1342 0
000-209600-13410
GOCI'20B6Q0-13S4
Data Issued
11120.2015
1120.2015
1120i2015
1120.2015
11i20i2015
1120.2015
11(20.2015
11202015
09-15S014
06.2fl.2013
0®2fli2013
06.2«a013
BO-Day Response
02/28/2016
02/282010
0228/2016
02282016
02282016
0228/2016
0228/2016
02/28/2016
014)32015
10*042013
1004/2013
10042013
SO-Oay Response
Pcr>d*»fl i.
F'endjvj Jt
StiCtesSftaly Traiismffled to OPP J.
Liasaffia,* I
SuetesiKily Transfflffled to OPP ±
Pending £
SuetessAiHv TianwniOed to OPP £
No At lion Available
Pendevfl ±
Pendant) JL
Fendetfl Jt
No Ai ton Available
Data Submission
No Action AvataMe
No Action Avaiable
Pending
No Action Abatable
Pending
No Acton Available
Pending
No Acton Abatable
No Acton Avalable
No Acton Avaiabie
No Acton Avaisbie
No At ton Ayaiable
Exhibit 12-21: DCI List After Submission
In addition, you will receive an email stating that your 90-Day Response Submission was
successfully transmitted to OPP. An example of this email is seen below in Exhibit 12-22.
Your 90-Day Response Submission (GDCI-101101-1972) has been successfully transmitted to OPP and is
awaiting processing. Your tracking number is CDX_DCI_2016_000003.
Below are the guideline(s) included in this response:
Acute dermal irritation - 870.2500
21/28-day dermal toxicity - 870.3200
90-day dermal toxicity - 870.3250
Once your 90-Day Response is processed by OPP, you can start additional data submission.
Company Name: TEST ORG
Company Number: 123
If you have questions concerning this message, you may contact the CDX Help Desk by email at
helpdesk@epacdx.net or by calling the CDX Technical Support Staff through our toll free telephone
support on (888) 890-1995 between Monday through Friday from 8:00 am to 6:00 pm EST/EDT. For
International callers, the CDX Help Desk can also be reached at (970) 494-5500.
CDX Homepage
https .//cdx.epa. gov
United States Environmental Protection Agency - Central Data Exchange
Exhibit 12-22: GDCi 90-Day Response Email Notification
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12.5 PDCI 90-Day Response
The following sections detail the process of completing and submitting a PDCI 90-Day
Response. PDCIs may contain multiple EPA Registration Numbers. Unlike GDCIs, the
guidelines are grouped under each EPA Registration Number. This allows you to respond to the
guidelines differently based on the EPA Registration Number provided.
If you choose to cancel a product registration, you will not have to fill out any of the guidelines
associated with that registration. However, the other product registrations and their guidelines
will remain unaffected. Please refer to the subsequent PDCI sections for more details.
IMPORTANT: If you forget the passphrase to your DCI, you will be unable to access it. For
security reasons, the system administrator does not have access to the passphrase and will not be
able to retrieve it or reset it to a new one. To prevent losing access to submissions, OPP suggests
that each company agree upon and use the same passphrase for all submi ssions. A shared
passphrase also allows users within the same company to perform submissions for others if
needed. If the original creator of a submission (either completed or in draft) is unavailable for
whatever reason, the shared passphrase ensures that someone from the same company can
retrieve and/or complete the submission. OPP will be unable to retrieve or unlock the submission
for the company. The same passphrase must be used throughout the life of the DCI.
12.5.1 PDCI 90-Day Response Submission Screen
After clicking the 'Start 90-Day Response' link, you will be navigated to the '90-Day Response
Submission' screen. This screen contains summary information about the DCI. You can also
upload DCI-level documents on this screen. A navigation tree is also present, pictured below in
Exhibit 12-23.
ft DCtHumtoer
FDCM01101-1902
f '=•:> Day Re»p702600. 870 S2O0. 870 5240
- Document Type Okov 9 0o<
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Exhibit 12-23: PDCI Navigation Tree
Since the '90-Day Response Submission' screen is the same for both GDCIs and PDCIs, please
refer to Section 12.4.1 for a detailed description of the items on this page.
Navigation: Review the displayed information and upload DCI level documents if desired. Click
the 'Next' button.
Note: For information about the 'Save,' 'Preview,' 'Validate,' and 'Submit' buttons in the
Application Footer, proceed to Section 5.4. Otherwise, proceed to the next section.
12.5.2 PDCI EPA Product Registration Screen
This screen contains basic information about an EPA Registration Number. On this screen, you
may choose one of three radio button options. Select a radio button option for each EPA
Registration Number (if more than one) before proceeding to the 'Requirement Status &
Registrant Response' section.
The following information is displayed on the 'EPA Product Registration' screen:
•	EPA Registration Number: The EPA Registration Number associated with the DCI. This
field is not editable.
•	Product Name: The Name of the product associated with the DCI. This field is not editable.
The following radio button options are available:
•	I wish to cancel this product registration voluntarily: Selecting this option will cause a
file upload section to appear.
Exhibit 12-24 below demonstrates this selection. A document must be uploaded to support
the cancellation. Click the 'Add Document' button, choose a 'Document Type' and
'Subtype' and upload a document via the 'Browse...' button. Any uploaded documents will
appear in the documents table in the center of the screen. You can delete added documents by
pressing the red 'Delete' icon in the ' Action(s)' column. The document types are as follows:
o Correspondence
¦ Company Letter
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General Correspondences

o
EPA Product Registration (EPA Rag. No. 352-596)
x r««itaiKt i CPAfieg Mo Jtt-439
Acute affinal nsauon
870J5CO
21f2#-«J3) ®srrj) Ion
BfO 3300
00-4JH  2500
Study TM*	.Acute Oeimai *>«!«
Tj-'jh Submn«orv Data	CIT.W2016
PUM&C-Ol	H
Patltrn	AA DC ft O
Tut Subsune*	EP MP TGAi
EPA *roeu
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CDX.
Navigation: Since no guidelines under this EPA Production Registration Number require a
response, you may click the 'Next EPA Registration Number' button to proceed to the next
registration number.
•	My product is ail MUP and I agree to satisfy the MUP requirements on the attached
form entitled "Requirements Status and Registrant's Response: Selecting this option
requires no additional data. Exhibit 12-26 below demonstrates this selection. After selecting
this option, click the 'Next' button; you can continue navigating through the DCI.
•	My product is an EUP and I agree to satisfy the EUP requirements on the attached
form entitled "Requirements Status and Registrant's Response: Selecting this option
requires no additional data. Exhibit 12-26 below demonstrates this selection. After selecting
this option, click the 'Next' button; you can continue navigating through the DCI.
ft DCI Numbtr
POa-191181-1 w
* 90-Osii Response Suomtsscn
I y~ |. EPA Reg *>. 352-WG
*roj»oo
Osrmal tauc*>r -
SW) 3200
99-art Oennattaoclly •
e«l 3230
ePAftag m
-	Acule dermal imaticri
8T02500
-	2UJWH 0»rmal Marty •
8*13300
EPA Product Registration |EPA Reg. No. 352-596)
si option)
SS2-SW
DUPOMT CANOPY 5P
n Y{iu mil not nave 1o M out any
«t mtt pa le^sssatton v and I agree to satisfy ihe MUP <*
in [ho aUctica torn enottM fSitjwremonls Sutws ana f&gs-.rar.Ts
My prodnn e an EUP 3rd J agree 3d me SUP
its on the attached ?orm enflttrt "Reqwrements Sa&s ant) fteassrars's Response'
Msaw OPwtw* ^vswme GSSutafl
Exhibit 12-26: MUP Option
Navigation: After selecting this option, click the 'Next' button to respond to the guidelines
within the DCI as seen below in Exhibit 12-27.
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r%
ocau hop •
ft DCI NumMr
PDCM011«M»t
f- 90 Day fteipcene Suwm»s**i
I | ; ePABm NO 352-5W
Acute Oei«TUil MiiMioa
srozsoo
2\0t-t9f oermal ttuialv -
8X0 3200
vo-aty Mm*i toueify -
¦90.3290
A- EPA ftetf Ho S5J-4W
Aeuie Ueimol niMtKn
tTQISQO
derma) ~ewer,
•70 S?00
90-OJj dermal Wucrty -
KT0 3JSO
L-1 AodCMnal Cmd Rtaptentt
EPA Product Registration (EPA Reg. No. 352-5%)
rtease idee! 1!>e apfopiuftf oprcn oettw Qntj or«e option can fte lefctwa
iryou tftooj# MKaixet sue product roowrauoti im« option) cfcsac upload s^pporeng,»
epa R*g Ml ration n
362-m
DUPOHT CANOPY SP HSRBlClO€
Mv product 18 in m jp and I agree to satisfy tiw MUP tequrements on me amcfieo fcrm ensued "Re31 »sjiw W s#W> ine EU"3 te-jurtnwnu o>
m entWrt "Hie^ements ®W una Re^wianr* RespciK *
Maaxe OPMt*s» /VWW CJ Sj
Exhibit 12-27: EUP Option
Navigation: After selecting this option, click the 'Next' button to respond to the guidelines
within the DCI.
12.5.3 PDCI Requirements Status and Registrant's Response Screen
This screen contains information about a Guideline Number within the DCI. On this screen, you
may choose a response from the 'Registrant Response' dropdown. After selecting a response,
additional fields or a document upload section may appear so that you can submit data to support
your response. You may also enter comments about the response into the 'Comments' text box.
You must respond to all guidelines before submitting the 90-Day Response.
The following information is displayed on the 'Requirements Status and Registrant's Response'
screen:
•	GuideLine Number: The Guideline Number associated with the DCI. This field is not
editable.
•	Study Title: The study associated with the guideline. This field is not editable.
•	Target Submission Date: The targeted date for submission. This field is not editable.
•	Protocol: The protocol for the guideline. This field is not editable.
•	Use Pattern: The use pattern for the guideline. This field is not editable.
•	Test Substance: The test substance for the guideline. This field is not editable.
•	Time Frame (month): The time frame for the guideline. This field is not editable.
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You may select a response for the guideline via the 'Registrant Response' drop down. You
may also copy a response to all guidelines under that EPA Product Registration Number by
clicking the blue icon next to the 'Registrant Response' drop down and clicking 'OK' in the
pop-up window. Please note that this will only copy the response to the guidelines grouped
under that particular EPA Product Registration Number. This will ensure that all guidelines
under a specific registration number have the selected response applied to them. You can later
change the response for the affected guidelines if you wish. See Exhibit 12-14 in the GDCI
section above for reference.
The possible responses for 'Registrant Response' are:
•	Developing Data: Selecting this response indicates that you will provide study data at a later
date. There is no document upload or data required as part of 90-Day Response submission
for this response. If you choose 'Developing Data,' you can click 'Next' to proceed to the
next guideline.
•	Agreement to Cost Share: This response requires at least one 'General Correspondence'
document upload. When selecting a response that requires a file upload, there are two radio
buttons available. The 'Add New Document' radio button should be used when you want to
upload a new document to the response. Click the 'Add New Document' radio button. The
document types are as follows:
o Form
¦	Form 8570-32 Certification of Attempt to Enter into an Agreement with
other Registrants for Development of Data.
o Correspondence
¦	General Correspondences
Select the 'Correspondence' document type and the 'General Correspondences' subtype. Enter
any comments if necessary. Upload a document via the 'Browse...' button. Click the 'Save'
button. The uploaded document will appear in the documents table in the center of the screen.
You may delete an uploaded document by clicking the red 'Delete' icon in the ' Action(s)'
column. After uploading a document, you will not be able to change your 'Registrant
Response' selection. You will have to delete all uploaded documents before you can change
your response. See Exhibit 12-15 in the GDCI section above for an example. Exhibit 12-16 and
Exhibit 12-17 above also detail the 'Use Previously Uploaded Document' radio button.
•	Offer to Cost Share: This response requires at least one 'General Correspondence' and one
'Form 8570-32 (Certification of Attempt to Enter into an Agreement with other Registrants
for Development of Data)' document upload. This response has the same document types as
'Agreement to Cost Share.' Upload the necessary documents and click the 'Next' button to
proceed to the next guideline.
•	Submitting Existing Data: This response allows you to upload study documents. It features
the standard file upload feature, but also allows you to enter an MRID for your study via the
'MRID' field. For assistance with generating a root MRID, please refer to Section 4. The
document types are as follows:
o Study
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¦	Data Entry Spreadsheet Template (DEST)
¦	Data Waiver Request
¦	Protocol
¦	Study
¦	Study Profile
¦	Supplemental Study Data
¦	Transmittal Document
¦	Water Monitoring Data
Upload all necessary documents and click the 'Next' button to proceed to the next guideline.
See Exhibit 12-18 in the GDCI section above for reference.
Note: The MRIDs you enter will be validated during submission or when you press the
'Validate' button within the Application Footer.
•	Upgrading a Study: This response allows you to upload study documents. It features the
standard file upload feature, but also allows you to enter an MRID for your study via the
'MRID' field. For assistance with generating a root MRID, please refer to Section 4. This
response has the same document types and features as the 'Submitting Existing Data'
response.
•	Citing a Study: This response allows you to cite studies. It features an 'MRID Number' field
so that you may enter the MRID of the studies you are citing. You can click the 'Cite an
additional MRID Number' link to cite multiple studies. You can also delete MRIDs by
clicking the red 'Delete' icon next to the MRID Number. See Exhibit 12-19 in the GDCI
section above for reference.
•	Waiver Request: This response features the standard file upload feature. The document type
and subtype are as follows:
o Correspondence
¦	Waiver Request
Upload the necessary documents and click the 'Next' button to proceed to the next guideline.
•	Not Applicable: This response features the standard file upload feature. The document type
and subtype is the same as the 'Waiver Request' response. This response also features an
'MRID' field so that you may enter an MRID. Upload the necessary documents and click the
'Next' button to proceed to the next guideline.
12.5.4 Additional Email Recipients and GDCI Submission Process
After all guidelines have been responded to, you may indicate additional email recipients on the
'Additional Email Recipients' screen. This screen allows you to indicate additional email
addresses to which DCI notification emails will be sent. By default, these emails are only sent to
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the PSP account that performs the submissions. These emails will inform the recipients when 90-
Day Responses and Data Submissions are submitted to OPP.
Click the 'Add a new email address' link. An 'Email Address' text field will appear. Enter the
email address of the desired recipient. If you would like to add more than one email address,
click the Add a new email address' link as many times as necessary. You can use the red 'x'
icon in order to delete entered addresses.
Once you are finished entering email addresses, click the 'Submit' button to begin the
submission process. Press 'OK' in the pop-up that appears. See Exhibit 12-20 in the GDCI
section above for reference.
Please refer to Section 10 for assistance with the submission process. After you have
successfully submitted the DCI, you will be navigated back to the 'DCI List' screen. Your
submitted DCI will have a status of 'In Transmission.' You will be able to submit data once your
DCI status changes to 'Successfully Transmitted to OPP.' See Exhibit 12-21 in the GDCI section
above for reference.
In addition, you will receive an email stating that your 90-Day Response Submission was
successfully transmitted to OPP. An example of this email is seen below in Exhibit 12-22.
12.6 Submit Data
The 'Submit Data' feature of PSP allows you to submit additional documents after you have
submitted a 90-Day Response. These additional documents will support previous responses and
help satisfy guidelines. You may submit data at any point after submitting a 90-Day Response.
The 'Submit Data' feature functions the same for both GDCIs and PDCIs.
Navigate to the 'DCI List' screen. Before you can submit data, the status of your 90-Day
Response submission must be 'Successfully Transmitted to OPP.' Click the 'Submit Data' link
in the 'Data Submission' column. See Exhibit 12-28 below for reference.
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Ackncwfcflgemcrrt" tnK in »ie cwrospMidng column
Allot lh« OP Atktvowledaon'iam is trarv.rruned to GPP, you may Mart a flQ-Oay R^tp&ni* Pleas* ckk on th
Response" fcrtts n the corraspondng column
After Die rn-tial BQ-0ay Response i& siKt«»tu»» vansmrtlcd w and pme-sscd by OPP you may sun a
chck on (he "SuCctii Data* imk m me ttwre-sponding tcJunwi You may submit mu&ple times to SiMsfy al
You tun view and rtM a DC IA
downtotai a copy OH record
la Submission Please
x Data Submission before subnimna AHe« submittal, you n
No Action Available: No acbon is available lei this Type ot response
No Action Needed: Tlio is a legacy DO. you don't need to sutiml! OCI AtkniyMedgeroent and Intel 90 Day Response
A waning U»«f Compltilon: rue Response o ri pi ogress and has no4 Deen submitted yei
Faded Validation: The Reipqnw liafc vaMabon crws and cannot fce submitted
hi Transmission: The Response it n Iransmmicn from DCM » OPP
Pending: The package has been tansmffled to OPP and a awafeng processing
Failed Transmission to OPP- The Response taded transmission to OPP
Swcee iiluify Transmitted u> OPP. I ho Response was toccesclbty iranwraied ami processed By OPP
Start PCI Ack nowledgamant: s-jfcma an acknowledgement thai yog have receded ttie Dasa Can-In from EPA
Start 9(5-Day Response: Su6m« a 00-Day R«poiv*e for the Onsa CaUft
Submit Data: Subm« add)t»rtal data la support your responses and safety gwdeenes
Submit Data (Previous Submission Successful]: Subrt-* addflcrnal data Vour previous suemtvsem was sustm
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CDX.
Exhibit 12-29: Data Submission Screen
Navigation: Add additional DCI Level Documents if desired by clicking the 'Add DCI Level
Document' button. Proceed to the next set of guidelines to submit additional documents.
The 'Data Submission' portion of PSP allows you to re-enter your 90-Day Response and upload
additional documents to satisfy guidelines. All previously entered data will be displayed.
However, you will not be able to change any of your responses as seen in Exhibit 12-30 below.
Any previously submitted documents will have a status of 'Previously Submitted' in the
' Action(s)' column. For assistance with uploading documents to a response, please refer to
Section 12.4.3 for GDCIs and Section 12.5.3 for PDCIs.
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ft OCIN«mbtr
POCt-101T01-1903
i Dirts Sutmttwon
f EPAR«a No 3«-6W
i- EPARetf No M2-4M
I acuip dermal ¦mason ¦
870 2500
I 2148-day demiad to***
870 3200
80-day dermal to«:«y
&70 32&0
Additional £mal Rec*>«nit»
So loci a iirvponw? tiom ttie "HegrtWanr*
£i»Mxmnt'drop down Seleci a documeni
type and upload » wpportng document«
T#*t SutHtance EP TOAI
Tim* Frame (month) ?4
d (or food usifs i either oi 9>r lotowirig catena « met iij the use
l>a«em n such Bias (he dermal rou!e «voukl be Hie primary route ofenpimire oi
(») »ie attoe miyieijJSiM a known ot e«pee
¦ Decuman* Subtype
lite Previously Uploaded Document
i#e a Document Subtype	»
M Save OPrctww ~ Vakiatc Q Subrrtf
Exhibit 12-30: Data Submissions
Navigation: Upload any additional documents and click the 'Next' button.
The submission process for a Data Submission is the same as the 90-Day Response. Please refer
to Section 10 for assistance with the PSP submission process. When you successfully submit a
Data Submission, the 90-Day Response copy of record is updated on the 'DCI List' screen. The
copy of record is additive, it will show all the documents submitted as part of the 90-Day
Response or subsequent Data Submissions. Please refer to Section 12.7 for assistance with
accessing the copy of record. You can make another data submission after your previous data
submission successfully transfers to OPP. However, you will not be able to submit additional
data until the status changes to 'Submit Data (Previous Submission Successful).' You can submit
data as many times as is necessary to satisfy all guidelines. See Exhibit 12-31 below.
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*S> OC11st Help •
Pgrlol	
AelmQMMganwnr irk m Bie cwMpotidrtg cofconn
After IheDCi Ac kn»uwleiSs*[nenl is tiarvsmrtled to OPP yau muy start J 90 Ojy Response Please ckk on Die "SlartW Day
Response" tax in the corresponding column
After t|i« initial S0-0ay Response « su«*«4u#y Vaitsmifliid to .vnd pox»y Response
A waiting User Completion Th* Respond is 2&Q0I6
02292010
02202016
032&20I6
022&20I6
0328/3016
01/032015
10.042013
10.042013
10/042013
flC-Oay Response
Pendng i
Pendng £
Successful Transmuted » OPP ±
Succosshjly Transmuted to OPP JL
Successfa»y Transmitted Ho OPP Jl
Pondnjj Ji
Successful Tiansimtted to OPP ±
No Action Available
PfifJWMJ X
Penary £
P«ndng JL
No Action A variable
k) Acton AvaMt*
^PmweiJ^&ibm«tiw^uccessMj
la Ac son AvaJabSe
In AcQon AvailabWi
Mki Ac Son Available
COX links *
Exhibit 12-31: Submit Data (Previous Submission Successful)
Navigation: Click the 'Submit Data (Previous Submission Successful)' link to start another data
submission. You can do this as many times as necessary until all guidelines are satisfied.
12.7 DCI Copy of Record
Once you submit a DCI Acknowledgement or 90-Day Response, you will have the ability to
download a copy of record. To download a copy of record, click the green 'Copy of Record' icon
in either the 'DCI Acknowledgement' or '90-Day Response' column on the 'DCI List' screen.
See Exhibit 12-32 below for reference.
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1
You must have a Data Call In from EPA to start a DO AcluicnfedgerneM To start a DCI Acknowledgement. t kk on me "Sun DC!
Aeitiovrtetlgiwnenr irk ei oic cancspontkeg column
t may *lart «£<0-D»y Re'.pon'.e Pfrav ekk, on the "St.M! vO Dity
After Uie OCl At MrowletigerTterYi a Inknynrtied to OPP y
Re-ipoirw" Mk n tt» coneipondaig column
Mter ttwi mttul fiO-Oay Response tvsuccessiuky oansmtotti to and proeess« by 0?V you may wan a Data Suarnsstn P*/w«
cfckon tfve "Submit Data* tak m ho tonesponS/vg column Vou may tubiwemutate !m«t 10satisfy al r#^u«»m*nts
You cam view and e-dit a OCl Acknowledgement 90-Day Response or Data Submission beiore subrrBOmg After vubtrffing. you ma
Qau Call-in A Rat pons* Legend
No Action Available: No uc«eri« available ftw this Vype ot response
No Action Needed: Tha is o legacy OCl. you tfonlneed to subm* DCI Atknuv-tedoemerii and irftaiM-Day Respoi'w
Avralttng liter Compla Hon 'he Response if *» progress and Jias rvoi been su-timnru vol
Failed Validation: I hp Response ha* vaWatton errors ana cannofl be submenu)
In Transmission: ftie Response is 0 transmission 10 OPP
Successfully Transmitted »a OPP: I fie Response- was successlut* transmuted and processed by OPP
Start DCI Acknowledgement: ikitonit on acfctwiyteiSflemenl I twit you have itttvett Bif Data Cal ln (rem CPA
Start tS-Oay Response -Subrert a &0-Day Response (or Hie Data Call In
Submit Data: submt additional data to snipped your responses anil sawfy guajelnet
Submit Data [Previous Submission SueeesstuS]: Sutim* additional data Your jirevaous subir^.sion was success&jt*
id to OPP
Company Namt; TESTQRCM123)
OCl Number. ALL 	• OCi Acknowledgement Status: AIL	ej M-Oay Response Status: ! ALL	ej	Items Per Page: S *
1? entnes Icund
DCI Numbef •
Da.aH.ued
• 50-Day Response Deadline •
DCI Acknowledgement » SQ-Oay Response
•
Dau Submission
GDCMOUCU-66573 0
1100*2016
02/2&20T6
Pendeig
i
-••-r.'j r:i|i 1

Ho Acoon Ayaiacte
P0CH01101-16090
11(280016
02/23/2016
P*nd*is
1
"'end r 111 |

No Aeten Avabble
QOCMOIIOI-WW©
11WM15
o?/2«wie
Pending
±
Successfcjiy TtaiHminwi to OPP i

Pending
GOCI-1O11O1-t9B6 0
Ilf20e20i6
02/28/2018
PWd«fl
±
SucceaslUty Franwnittnfl to OPP J.
SubmaDi
11a (Previous Sutxnn-scr* Successful
PDcuonoi-ieioo
11/208015
02<28'2016
Pendmg
L
Suecesslkjly Transimined to OPP jL

Pend*>g
<5OCt-iDl1oi-te«0
11130Q01&
02/28'201S
Pendmg
±
Pnnitng i.

No Action AwMlile
PDCU01101-19110
11/20/2015
02/2^-2018
Pendmg
±
Successful Tiansmitied to OPP 1 Pending
POCMOf 101 -19981
t1i«W0t5
0238-201«


lomeM No- Acton Av.iiabie

No Action Ava&Uifat
P0C1.111801.360760
09MW014
0103/2016
Pend«o
i
Pcnffirtfl ±

No Action AyataOle
GOCI-2M600-1342 0
Q"3,2&2013
1 (MM/2013
Pending
±
Peniimg A

No Acbon AvjwMe
GOCI-2O96OO-13410
06/20/2013
KV04«013
P*«d«tg
±
Pondmg -1

No Acton Avalafcle
COX Link* •
Exhibit 12-32: 'Copy of Record' Icons
Navigation: Click the green 'Copy of Record' icon in the 'DCI Acknowledgement or '90-Day
Response' column.
After clicking the 'Copy of Record' icon, you will be navigated to the 'Cross-Media Electronic
Reporting Regulation (CROMERR)' screen. You will have to enter the passphrase used to
encrypt the submission, your CDX password, and the answer to one of your secret questions to
see the copy of record. See Exhibit 12-33 below.
Q XILS Hap
Cross-Media Electronic Reporting Regulation (CROMERR)
pihk Enter Passpnrase
Lcgntocox
tower seereiGBMiQn
DCI Number
POG-tflltlH-tW
P3SSpllJ3S«
user id
JWKTWTrST
Qustion
Vrtwl ft tl* 'M ard nitftSt1 nan* of yoir nkfctf sting?
Answf
sang
Exhibit 12-33: CROMERR Copy of Record Screen
Navigation: Enter the passphrase used to encrypt the submission, your CDX password, and the
answer to one of your secret questions. Click the 'Next' button.
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Note: Since DCI Acknowledgements do not require a passphrase, you will only have to enter
your CDX password and the answer to one of your secret questions.
After entering all the requisite information, you will be navigated to the 'Copy of Record' screen
as seen in Exhibit 12-34. Click the green 'Download Document' icon in the 'Action(s)' column
to download a copy of record for your submitted documents. You may also download a PDF
overview of your submission.
Copy of Record
C0B.TE3T OR0 2332 P«*
TrP*
EPAN0 34J.4W
JS2.4M mttOO
3SI-4W flT033»
in
®
Exhibit 12-34: Copy of Record Screen
Navigation: Click the green 'Download Document' icons to download the associated
documents.
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13 Appendix A - Definitions, Acronyms, and Abbreviations
Acronym
Full Name
CBI
Confidential Business Information
CDX
Central Data Exchange
CoR
Copy of Record
CRM
Chemical Review Manager
DCI
Data Call-In
CROMERR
Cross-Media Electronic Reporting Regulation Security System
EPA
Environmental Protection Agency
IT
Information Technology
MRID
Master Record Identification Number
OPP
Office of Pesticide Programs
PDF
Portable Document Format
PRIA
Pesticide Registration Improvement Extension Act
PSP
Pesticide Submission Portal
SLN
Special Local Need
XML
Extensible Markup Language
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14 Appendix B - Admin Number Information
Admin Number Information
The EPA Registration Number (Admin Number) is required on all pesticide products. The
purpose of an Identification Number is to provide a unique product number for regular
registrations, distributor registrations, Special Local Needs registrations, and Experimental Use
Permits.
The EPA Registration Number indicates which company holds the registration for the pesticide
product, and in which sequence the product was submitted to EPA by the company.
Refer to Exhibit 14-1 below for examples of Admin Numbers. Please note the following:
•	CompanyNum = Company Number
•	xxSEQxx = Sequence
•	Seq = Sequence
•	ParentRegNum means = Parent Regulatory Number
•	EUP = Experimental Use Permit
•	IN = Inert Ingredient Request
•	PA = Pre-Application
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Regulatory Action
Format
Examples
Product Registration - Section 3
CompanyNum-xxSEQxx
•	55050-1
•	334-165
•	334-ANA (Temporary File
Symbol before the product is
registered, see Exhibit 12-2)
Distributor Product
ParentRegNum-CompanyNum
•	2155-40-12319
•	3862-140-13103
Experimental Use Permit - Section
5
CompanyNum-EUP-xxSEQxx
•	44544-EUP-2
•	45054-EUP-1
Tolerance Petition
ParentRegNum-CompanyNum
•	3F1383
•	2G1214
•	Possible 2nd characters:
E,F,G,H,T - based on the
Tolerance Petition type
Inert Ingredient Request
As given below 2nd character being
E,F,G,H,T based on the tolerance
petition type
•	IN-10606
•	IN-10559
Pre-Application
CompanyNumPASeq
•	2382PA1
•	54022PA16
Exhibit 14-1 Admin Number Examples
R
E
G
U
L
A
T
I
O
N
1
2
3
4
5
6
7
8
9
0
Exhibit 14-2 File Symbol
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