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Pesticide Registration Improvement Renewal Act (PRIA 2)
Fee Determination Decision Tree

Note: EPA no longer updates this information, but it may be useful as a reference or resource.

Decision Tree Resources:
Below is the fee for your selected Fee Category for
Fiscal Year 2011 & 2012

Action Code
Description
FY11/FY12
Fee
FY11/FY12 Decision Time
(months)
A530
New product; identical or substantially similar in composition and use to a registered product; no data review or only product chemistry data; cite-all data citation, or selective data citation where applicant owns all required data, or applicant submits specific authorization letter from data owner. Category also includes 100% re-package of registered end-use or manufacturing-use product that requires no data submission nor data matrix.
$1,159.00
3


Do you plan to request either of the following types of waivers?

50% waiver 50% waiver
75% waiver 75% waiver

To pay the fee shown above, go to http://www.pay.gov and follow the instructions.

How to submit your application directly to EPA.


Action Code Interpretation: An application for registration of an end-use or a manufacturing use pesticide product that is substantially similar, identical in its uses and formulation or that differ only in ways that would not significantly increase the risk of unreasonable adverse effects on the environment to products that are currently registered. The applicant must identify the similar products for all active ingredients in the proposed product.

All applications require the following:

  • A data matrix is required with the application if it is not a 100% re-packaged product.
  • Product chemistry data (Group A and B) unless the product is identical (e.g. 100% repackaged product).
  • The active ingredient listed on the CSF must be an EPA registered product.
  • In all cases, the registrant must identify the registered similar product for this category.
  • Acute toxicity requirements must be addressed by using:
    1. the cite-all method
    2. selective data citation where the applicant owns all required data, or
    3. applicant submits specific authorization letter from the data owner.

The application is not in this category if efficacy, acute toxicity, companion animal safety, and/or child resistant packaging data are submitted and must be reviewed to support the application. The application does not fall into this category if it contains a request to waive any of these data. An application that requires review of cited or submitted data other than product chemistry does not belong in this fee category. If the use pattern on the TGAI differs from the proposed products, then additional data are required and the application does not fall within this category.

Substantially similar: Product must have the same active ingredient, in substantially the same proportion, same chemical composition (solid, liquid, granular), and substantially similar inert ingredients as the already registered product,. In addition, substantially similar means that the product bears the same use patterns or fewer. Adding to or changing existing use patterns excludes the product from treatment as a substantially similar product. Substantially similar use patterns for public health products are limited to identical organisms on both products. For non-public health products substantially similar use patterns are limited to identical organisms on both products.

Deleting use patterns is acceptable

Identical products: Same composition and use patterns as an already registered end-use product.

Manufacturing Use Product: A 100% re-package of a manufacturing use product that requires no data submission nor data matrix is covered by this category.

Unregistered: The Agency has not issued an EPA Registration Number (license) for the source material.


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