Skip to main content
An official website of the United States government
The .gov means it's official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you're on a federal government site.
The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.
Search:
Agenda
Reg Review
ICR
This script is used to control the display of information in this page.
Display additional information by clicking on the following:
All
Brief and OIRA conclusion
Abstract/Justification
Legal Statutes
Rulemaking
FR Notices/Comments
IC List
Burden
Misc.
Common Form Info.
Certification
View Information Collection (IC) List
View Supporting Statement and Other Documents
Please note that the OMB number and expiration date may not have been determined when this Information Collection Request and associated Information Collection forms were submitted to OMB. The approved OMB number and expiration date may be found by clicking on the Notice of Action link below.
View Generic ICR - OIRA Conclusion
OMB Control No:
2070-0174
ICR Reference No:
202106-2070-001
Status:
Historical Active
Previous ICR Reference No:
201801-2070-003
Agency/Subagency:
EPA/OCSPP
Agency Tracking No:
2288.04
Title:
Pesticides Data Call In Program (Renewal)
Type of Information Collection:
Revision of a currently approved collection
Common Form ICR:
No
Type of Review Request:
Regular
OIRA Conclusion Action:
Approved without change
Conclusion Date:
12/28/2022
Retrieve Notice of Action (NOA)
Date Received in OIRA:
11/30/2021
Terms of Clearance:
In accordance with 5 CFR 1320, the information collection is approved for three years. Prior to the next renewal, OMB requests that EPA evaluate and begin efforts to implement the received public feedback (e.g., allow all forms to be prepared and submitted electronically, allow electronic signature on all forms, reconsider the use of Forms 8570-36 and 8570-37). Refreshing the initial Terms of Clearance, under this approval, DCIs must be approved by high-level management (Deputy Division Director or above). Before EPA may issue a specific DCI under this approval, EPA must submit the DCI to OMB, and OMB must approve the DCI. The information sent to OMB must include basic information on the pesticide, the total number of respondents, the planned schedule for issuance and data submission, a list of required studies, the practical utility of the data, and an estimate of the paperwork burden and testing costs. OMB may request that EPA provide additional information as necessary to explain the basis for the DCI. OMB may also request that EPA issue a FR notice seeking public comment on the DCI. OMB does not commit to expedited review of a requested DCI, and OMB does not authorize EPA to proceed with a DCI automatically after a fixed number of days. Based on its review, OMB may determine that a requested DCI does not comply with the requirements in 5 CFR 1320 and may either return the request to EPA for reconsideration or disapprove the request. EPA may not issue the returned DCI until addressing the issues raised, resubmitting the request, and receiving OMB approval.
Inventory as of this Action
Requested
Previously Approved
Expiration Date
12/31/2025
36 Months From Approved
12/31/2022
Responses
283
0
472
Time Burden (Hours)
3,274,852
0
58,206
Cost Burden (Dollars)
0
0
0
Abstract:
This ICR covers the information collection activities associated with the issuance of DCIs under section 3(c)(2)(B) of the Federal Insecticide, Fungicide, and Rodenticide Act (FIFRA). EPA regulates the use of pesticides under the authority of two federal statutes: FIFRA (7.U.S.C. 136 et seq.) and the Federal Food, Drug and Cosmetic Act (FFDCA) (21 U.S.C. 346). In general, before manufacturers can sell pesticides in the United States, EPA must evaluate the pesticides thoroughly to ensure that they meet federal safety standards to protect human health and the environment. EPA grants a "registration" or license that permits a pesticide's distribution, sale, and use only after the company meets the scientific and regulatory requirements. In evaluating a pesticide registration application, EPA assesses a wide variety of potential human health and environmental effects associated with the use of the product. Applicants, or potential registrants, must generate or provide the scientific data necessary to address concerns pertaining to the identity, composition, potential adverse effects, and environmental fate of each pesticide. The data allow EPA to evaluate if a pesticide has the potential to cause harmful effects on certain non-target organisms and endangered species, and on surface or ground water. Through a scientific and public process, EPA specifies the kinds of data and information necessary to make regulatory judgments about the risks and benefits of pesticide products under FIFRA sections 3, 4 and 5, as well as the data and information needed to determine the safety of pesticide chemical residues under FFDCA section 408. The regulations in 40 CFR part 158 describe the minimum data and information EPA typically requires in an application for pesticide registration or amendment; reregistration of a pesticide product; maintenance of a pesticide registration by means of the DCI process (e.g., as used in the registration review program); or to establish or maintain a tolerance or exemption from the requirements of a tolerance for a pesticide chemical residue. EPA uses the DCIs issued under this ICR to acquire the data necessary for its statutorily mandated review of a pesticide’s registration, which assess if the continued registration of a pesticide causes an unreasonable adverse effect on human health or the environment.
Authorizing Statute(s):
US Code:
7 USC 136 et seq.
Name of Law: FIFRA
US Code:
21 USC 346a
Name of Law: FFDCA
Citations for New Statutory Requirements:
None
Associated Rulemaking Information
RIN:
Stage of Rulemaking:
Federal Register Citation:
Date:
Not associated with rulemaking
Federal Register Notices & Comments
60-day Notice:
Federal Register Citation:
Citation Date:
86 FR 16718
03/31/2021
30-day Notice:
Federal Register Citation:
Citation Date:
86 FR 67460
11/26/2021
Did the Agency receive public comments on this ICR?
Yes
Number of Information Collection (IC) in this ICR:
14
IC Title
Form No.
Form Name
#1- Reregistration DCIs: Confirmatory Data
See List
See List
#10- Anticipated Residue DCIs: Base set of Data
See List
See List
#11- Anticipated Residue DCIs: Updated Verification of Use Data
See List
See List
#12- Anticipated Residue DCIs: Updated Public Source Monitoring Data
See List
See List
#13- DCIs for Percent Crop Treated Estimates
See List
See List
#2- Reregistration: Voluntarily Submitted Data (Low Burden Studies)
See List
See List
#3- Reregistration: Voluntarily Submitted Data (High Burden Studies)
See List
See List
#4- Reregistration DCIs: Product Specific Data
See List
See List
#5- Maintenance DCI
See List
See List
#6- Registration Review DCIs
See List
See List
#7- Registration Review Resistance Management Plans
See List
See List
#8- Reregistration Review: Voluntarily Submitted Data (Low Burden Studies)
See List
See List
#9- Reregistration Review: Voluntarily Submitted Data (High Burden Studies)
See List
See List
DCI for Streptomycin Sulfate
6300-3, 6300-4
Data Call-in Response, Requirements Status and Registrant's Response
ICR Summary of Burden
Total Approved
Previously Approved
Change Due to New Statute
Change Due to Agency Discretion
Change Due to Adjustment in Estimate
Change Due to Potential Violation of the PRA
Annual Number of Responses
283
472
0
0
-189
0
Annual Time Burden (Hours)
3,274,852
58,206
0
0
3,216,646
0
Annual Cost Burden (Dollars)
0
0
0
0
0
0
Burden increases because of Program Change due to Agency Discretion:
No
Burden Increase Due to:
Burden decreases because of Program Change due to Agency Discretion:
No
Burden Reduction Due to:
Short Statement:
Estimates of burden hours and costs are substantially larger than in the most recent ICR. This is primarily due to an error in past ICRs where annual totals were misreported as 3-year totals underestimating the total approved burden hours and costs by a factor of 3. The Agency has corrected this error and is now reporting annual total burden hours and costs throughout this ICR. Additionally, due to a clerical error, a burden of 58,206 hours was approved rather than the submitted 625,669 burden hours from the currently approved ICR by OMB. The Agency has corrected these errors and this ICR represents an increase of 2,649,183 hours (3,274,852 – 625,669) in the total estimated annualized burden compared with what is currently approved by OMB. The burden increase is a result of several factors, including an increase in DCIs issued annually (Previous to Current Numbers), the addition of high-test costs for certain DCIs, and an increase in non-government wage rates. All these activities have contributed to the significant increase in burden.
Annual Cost to Federal Government:
$1,652,342
Does this IC contain surveys, censuses, or employ statistical methods?
No
Does this ICR request any personally identifiable information (see
OMB Circular No. A-130
for an explanation of this term)? Please consult with your agency's privacy program when making this determination.
No
Does this ICR include a form that requires a Privacy Act Statement (see
5 U.S.C. §552a(e)(3)
)? Please consult with your agency's privacy program when making this determination.
No
Is this ICR related to the Affordable Care Act [Pub. L. 111-148 & 111-152]?
No
Is this ICR related to the Dodd-Frank Wall Street Reform and Consumer Protection Act, [Pub. L. 111-203]?
No
Is this ICR related to the American Recovery and Reinvestment Act of 2009 (ARRA)?
No
Is this ICR related to the Pandemic Response?
No
Agency Contact:
Angela Hofmann 202 260-2922 hofmann.angela@epamail.epa.gov
Common Form ICR:
No
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:
(a) It is necessary for the proper performance of agency functions;
(b) It avoids unnecessary duplication;
(c) It reduces burden on small entities;
(d) It uses plain, coherent, and unambiguous language that is understandable to respondents;
(e) Its implementation will be consistent and compatible with current reporting and recordkeeping practices;
(f) It indicates the retention periods for recordkeeping requirements;
(g) It informs respondents of the information called for under 5 CFR 1320.8 (b)(3) about:
(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;
(h) It was developed by an office that has planned and allocated resources for the efficient and effective management and use of the information to be collected.
(i) It uses effective and efficient statistical survey methodology (if applicable); and
(j) It makes appropriate use of information technology.
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.
Certification Date:
11/30/2021