Pesticide Registration Improvement Extension Act (PRIA 3)
Fee Determination Decision Tree
Decision Tree Resources:
Below is the fee for your selected Fee Category for Fiscal Year 2013
| Decision Time
|R123||New Active Ingredient, Seed treatment only; includes agricultural and non-agricultural seeds; residues not expected in raw agricultural commodities (2) (3)||$ 427,991||18|
Do you plan to request either of the following types of waivers?
|50% waiver||You pay ---->>>>>||$ 213,996|
|75% waiver||You pay ---->>>>>||$ 106,998|
To pay the fee shown above, go to http://www.pay.gov and follow the instructions.
|Action Code Interpretation|
An application for seed treatment only that proposes a food use or non-food use for an active ingredient that is not currently contained as an active ingredient in any U.S. registered pesticide product that is not expected to result in residues in raw agricultural commodities. The application submission must contain a petition requesting the non-food determination. If a determination is made that the uses do not need a tolerance or exemption from the requirement of a tolerance, then the chemical will be listed in the 40 CFR 180.220 Non-Food Determination section. All uses (food and non-food) included in the original application for each new active ingredient are covered by the base fee for the application in this category if submitted in this package. In order for a food crop seed treatment to be considered in this category, data from a radiotracer study must be available showing no uptake of residues (radioactivity) from treated seed into the aerial portion of the growing crop. Guidance is available at http://www.epa.gov/ocspp/pubs/frs/publications/Test_Guidelines/series860.htm. If residues occur in the aerial portion of the plant, or if there is no data available to make this determination, seed treatments are considered to be food uses requiring tolerances and fall into a different category.
All of the inerts used in the product must be either approved, pending with the Agency, or a new inert is submitted within the package for the applicable uses.
A maximum of five new products are covered by the base fee. After the first five new products, each application for an additional new product or new inert ingredient approval that is submitted within this new active ingredient package is subject to the registration service fee for a new product or a new inert ingredient approval. All such associated applications that are submitted together will be subject to the new active ingredient decision review time. Any additional information that was neither requested nor required by the Agency, submitted at the applicant’s initiative after completion of the technical deficiency screening, and which does not itself constitute a covered registration application, shall be assessed an additional 25% of the full service fee.
The Agency will provide the applicant with a pre-decisional determination 4 weeks prior to the PRIA decision review time due date which specifies any label changes that have to be made in order to grant the requested new active ingredient registration. If the label issues cannot be resolved prior to the PRIA decision review time due date and if a PRIA due date time extension has not been agreed upon, then the Agency will issue to the applicant its regulatory decision with the specific label changes and supporting documentation on or just before the PRIA decision review time due date. At that time the applicant must either (a) agree to all of the label changes and submit a revised label that incorporates all of these label changes; or (b) does not agree with one or more of the label changes and request up to 30 days to reach agreement with the Agency and submit a revised label that incorporates all of the agreed upon label changes, which the Agency has 2 business days to review; or (c) withdraw the application without prejudice.
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