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
|M001||Study protocol requiring Human Studies Review Board review as defined in 40 CFR Part 26 in support of an active ingredient (4)||$ 7,200||9|
Do you plan to request either of the following types of waivers?
|50% waiver||You pay ---->>>>>||$ 3,600|
|75% waiver||You pay ---->>>>>||$ 1,800|
To pay the fee shown above, go to http://www.pay.gov and follow the instructions.
|Action Code Interpretation|
|This category includes study protocols submitted to EPA, in support of an active ingredient, which propose research involving intentional exposure of a human subject, as those terms are defined in 40 CFR parts 26.1102(d), (e), and (i). Worker exposure studies and insect repellant efficacy studies are the most common types of studies submitted to OPP that may meet the regulatory definition of “research involving intentional exposure.”
A protocol that describes research that would provide data to populate a generic database such as the Agricultural Handler Exposure Database (AHED) or the Biocide Handler Exposure Database (BHED) will not be considered a PRIA action because the data from this type of research are intended to support many active ingredients, and the resulting study would not be submitted in support of a particular active ingredient.
EPA will review both the scientific and ethical aspects of protocols covered by this category. If EPA determines that the protocol is of sufficiently high quality, EPA will submit its review of the protocol, together with the available supporting materials, to the Human Studies Review Board (HSRB). The HSRB will provide comment on both the scientific and ethical aspects of the protocol. EPA will consider the HSRB’s advice in determining whether to approve the protocol.
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