Experimental Use Permits (EUPs) for Pesticides (Renewal)
Extension without change of a currently approved collection
No
Regular
Approved without change
09/09/2019
08/15/2018
Upon re-submission, EPA needs to consolidate all the OMB control numbers associated with the PSP Portal (2070-0040, 2070-0142, 2070-0039, 2070-0182, 2070-0060, 2070-0044, and 2070-0024). The agency is reminded to include a burden statement on the initial online screen for all collection activities within the PSP Portal and to provide updated screen shots of the PSP Portal and associated form questions.
table that charts list comparision
Inventory as of this Action
Requested
Previously Approved
02/28/2021
36 Months From Approved
09/30/2019
10
0
10
567
0
556
0
0
0
The information collected through this ICR provides EPA with the data necessary to determine whether to issue an experimental use permit (EUP) under section 5 of the Federal Insecticide, Fungicide, and Rodenticide Act (FIFRA). FIFRA requires that before a pesticide product may be distributed or sold in the U.S., it must be registered by EPA. However, FIFRA section 5 authorizes EPA to issue an EUP to allow pesticide companies to temporarily ship pesticide products for experimental use for the purpose of gathering data necessary to support the application for registration of a pesticide product. The EUP application must be submitted in order to obtain a permit. Such reporting will allow the Agency to determine whether further action is needed to prevent unreasonable adverse effects to human health or the environment.
US Code:
7 USC 136c
Name of Law: Federal Insecticide, Fungicide, and Rodenticide Act
Annual respondent burden is estimated in this renewal to be 567 hours, which is a slight increase from the estimate in the previous ICR of 556 hours. This increase is an adjustment as a result of increased EUP submissions by program participants.
On behalf of this Federal agency, I certify that the collection of information encompassed by this request complies with 5 CFR 1320.9 and the related provisions of 5 CFR 1320.8(b)(3).
The following is a summary of the topics, regarding the proposed collection of information, that the certification covers:
(i) Why the information is being collected;
(ii) Use of information;
(iii) Burden estimate;
(iv) Nature of response (voluntary, required for a benefit, or mandatory);
(v) Nature and extent of confidentiality; and
(vi) Need to display currently valid OMB control number;
If you are unable to certify compliance with any of these provisions, identify the item by leaving the box unchecked and explain the reason in the Supporting Statement.