B673 PRIA Fee Category
PRIA 5 Fee Determination Decision Tree:
Biochemical or Microbial Biopesticide Active Ingredient - New Product Registration
Below is the fee for your selected Fee Category for Fiscal Years 2025-2026
Action Code | Description | FY'25-FY'26 Fee | Decision Time (months) |
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B673 | New product; unregistered source of active ingredient(s); citation of Technical Grade Active Ingredient (TGAI) data previously reviewed and accepted by the Agency; requires an Agency determination that the cited data support the new product. | $7,689 | 12 |
Do you plan to request eit5her of the following types of waivers?
Waiver | Pay | Amount |
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50% waiver | You pay ---->>>>> | $3,845 |
75% waiver | You pay ---->>>>> | $1,923 |
To pay the fee shown above, go to Paying PRIA Application Fees web page and follow the instructions.
How to submit your application directly to EPA.
Action Code Interpretation |
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An application for registration of an end-use or a manufacturing use microbial or biochemical pesticide product containing an unregistered source of an active ingredient (i.e., the active ingredient in the proposed product is not derived from an EPA-registered product) for which the data cited to fulfill all generic (active ingredient) data requirements have been previously reviewed and accepted by the Agency. If new generic data/waiver review is required, see category B672. For microbial pesticides this category does not apply when data to demonstrate similarity is needed to bridge to previously reviewed and accepted data, see Table 11 (New Active Ingredients). All inert ingredients used in the product must be EPA approved for the proposed use(s), pending approval with the Agency for the applicable uses, or included in an inert petition submitted within the package for the applicable uses. Each application for a new inert approval submitted in this package is subject to its own registration service fee. An application for a new end-use product using a source of active ingredient that (a) is not yet registered but (b) has an application pending with the Agency for review, will be considered an application for a new product with an unregistered source of active ingredient. Where the action involves approval of a new or amended label, on or before the end date of the decision review time, the Agency shall provide to the applicant a draft accepted label, including any changes made by the Agency that differ from the applicant-submitted label and relevant supporting data reviewed by the Agency. The applicant will notify the Agency that the applicant either (a) agrees to all of the terms associated with the draft accepted label as amended by the Agency and requests that it be issued as the accepted final Agency-stamped label; or (b) does not agree to one or more of the terms of the draft accepted label as amended by the Agency and requests additional time to resolve the difference(s); or (c) withdraws the application without prejudice for subsequent resubmission, but forfeits the associated registration service fee. For cases described in (b), the applicant shall have up to 30 calendar days to reach agreement with the Agency on the final terms of the Agency-accepted label. If the applicant agrees to all of the terms of the accepted label as in (a), including upon resolution of differences in (b), the Agency shall provide an accepted final Agency-stamped label to the registrant within 2 business days following the registrant’s written or electronic confirmation of agreement to the Agency. |