Pesticide Registration Improvement Extenstion 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
|A501||Additional non-food; indoor; FIFRA §2(mm) uses; 6 or more submitted in one application (4) (5)||$ 69,462||9|
Do you plan to request either of the following types of waivers?
|50% waiver||You pay ---->>>>>||$ 34,731|
|75% waiver||You pay ---->>>>>||$ 17,366|
To pay the fee shown above, go to http://www.pay.gov and follow the instructions.
|Action Code Interpretation|
|An application that proposes a non-food use for an active ingredient with a current EPA registration. A non-food use includes a proposed use that is not a “food use” as described in the food use categories. The product is for use inside a manmade structure or is a low exposure use pattern that requires minimal ecological and/or environmental fate data (see examples below) and that fits the definition of an antimicrobial found in FIFRA section 2(mm). 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 application must propose at least six (6) or more specific new additional non-food indoor uses.
All of the inerts used in the product must be either approved or pending with the Agency for the applicable uses.
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 use 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.
Amendment applications to add new use(s) to registered product labels are covered by the base fee for this category as long as they are all submitted in the same package. Each application for a new product and/or new inert approval submitted in this package, however, is subject to its own registration service fee. The only exception would be if the new use(s) were to be added only to a new product (no amendments to registered product labels in the application package) in which case the review of the one new product application would be covered by the base fee for the new uses. Any new product or amendment to the proposed labeling, which contains the same new use(s), that is submitted subsequent to the submission of the new use application but prior to its decision review time expiration date, will be deemed a separate new use application subject to a separate fee and new decision review time. Any other information not requested or required by the Agency, that is submitted by the applicant to support the new use(s) application, which is received 21 days or more after the original application, will be assessed 25% of the full registration service fee for the new use(s) application.
Finally, if the new use(s) application include non-food (indoor and/or outdoor) and food (outdoor and/or indoor) uses, the appropriate fee is due for each type of new use, and the longest decision review time applies to all of the new uses requested in the application.
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