B613 PRIA Fee Category
PRIA 4 Fee Determination Decision Tree:
Biopesticide Biochemical/Microbial Experimental Use Permit
Below is the fee for your selected Fee Category for Fiscal Years 2020-2021
|Action Code||Description||FY'20- FY'21 Fee||Decision Time (months)|
|B613||New active ingredient; petition to convert a temporary tolerance or a temporary tolerance exemption to a permanent tolerance or tolerance exemption (2)(3)||$18,428||11|
Do you plan to request either of the following types of waivers?
|50% waiver||You pay ---->>>>>||$9,214|
|75% waiver||You pay ---->>>>>||$4,607|
To pay the fee shown above, go to Paying PRIA Application Fees web page and follow the instructions.
|Action Code Interpretation|
An application that proposes a food use for a microbial or biochemical pesticide active ingredient that is not currently an active ingredient in any U.S. registered pesticide product. The use requires the conversion of an existing temporary/tolerance or exemption to a permanent tolerance under section 408 of the FFDCA. The application contains uses for food/feed commodities that are all currently covered by an existing tolerance or tolerance exemption and must contain a petition to establish tolerances or exemption(s) from tolerance for all food/feed commodities covered by the pending registration application(s). A different pattern of use that significantly changes or increases exposure such as a dosage rate increase or different method of application will result in the application being treated as a new use. The petition will not contain new data for review in this category. The agency will assess the risks associated with the conversion of the commodities. If conversion of a crop group or subgroup or commodities requires submission of new data, the action does not belong in this category. The appropriate category will be one of the food use categories (e.g. B580).
All uses (food and non-food) included in any original application or petition for a new active ingredient are covered by the base fee for the application in this category if submitted within the original application. Some examples of food uses include: use on foods, for example, corn or apples; aquatic uses involving potable water, irrigation, or requiring tolerances for fish, or shellfish; uses on areas where food may be grown or raised such as pasture, rangeland, home garden, beehive, and uses involving livestock, such as livestock housing, livestock dips, and livestock ear tags. 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.
Until the new active ingredient is approved, any subsequent application for another new product containing the same active ingredient or an amendment to the proposed labeling will be charged a new active ingredient service fee and decision review timeframe.
If the applicant on his own initiative submits any additional information that was neither requested nor required by the Agency, after completion of the technical deficiency screening, and which does not itself constitute a covered registration application, the applicant will be charged an additional 25% of the full registration service fee for the new active ingredient application.
The Agency will provide the applicant with a pre-decisional determination 2 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.