View Information Collection Request (ICR) Package
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View ICR - Agency Submission
COMMENT
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OMB Control No:
2070-0038
ICR Reference No:
202512-2070-004
Status:
Received in OIRA
Previous ICR Reference No:
202501-2070-008
Agency/Subagency:
EPA/OCSPP
Agency Tracking No:
1188.16
Title:
TSCA Section 5 Premanufacture Review of New Chemical Substances and Significant New Use Rules for New and Existing Chemical Substances (Renewal)
Type of Information Collection:
Extension without change of a currently approved collection
Common Form ICR:
No
Type of Review Request:
Regular
Date Submitted to OIRA:
12/31/2025
Requested
Previously Approved
Expiration Date
36 Months From Approved
01/31/2026
Responses
4,243
4,243
Time Burden (Hours)
129,367
129,367
Cost Burden (Dollars)
0
0
Abstract:
This information collection request addresses the reporting and recordkeeping requirements associated with both the new chemicals review and regulatory program and the existing chemicals program administered by EPA under section 5 of the Toxic Substances Control Act (TSCA), as amended by the Frank R. Lautenberg Chemical Safety for the 21st Century Act (the Lautenberg Act) (15 U.S.C. 2604). EPA is requesting to renew and consolidating two existing approved Information Collection Requests (ICRs). This consolidated ICR will cover information collection activities associated with Significant New Use Rules (SNURs) for both new and existing chemicals under TSCA. The information for SNURs and required notifications includes chemical identity, use and exposure information, test information and descriptions of other information related to the effects on health and the environment of the manufacture, processing, use, distribution in commerce and disposal of the new or existing chemical substance. This ICR is required for the information to be collected under notices for Significant New Use Rules for new and existing chemicals.
Authorizing Statute(s):
US Code:
15 USC 2604
Name of Law: Toxic Substances Control Act / Manufacturing and processing notices
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:
90 FR 19713
05/29/2025
30-day Notice:
Federal Register Citation:
Citation Date:
90 FR 61147
12/30/2025
Did the Agency receive public comments on this ICR?
Yes
Number of Information Collection (IC) in this ICR:
17
IC Title
Form No.
Form Name
Bona Fide Intent Notifications (Bona Fides)
7710-25
PMN
CDX Registration
Existing Chemicals Activities
7710-25
PMN
Instant Photographic Film Articles
Low Volume and Low Release/Low Exposure Exemptions (LVE/LoREX)
7710-25
PMN
Microbial Commercial Activity Notices (MCAN)
6300-07
BioTech
Notice of Commencement
7710-56
NOC
Polymer Exemption Post-Manufacture Annual Reports
7710-56
NOC
Premanufacture Notice
7710-25
PMN
Research and Development Exemption
7710-25
PMN
Section 5(e) Orders with Pended Testing/ 5(f) Orders with No Testing
7710-25
PMN
Section 5(e) Orders with Triggered Testing
Significant New Use Notice (SNUN)
7710-25
PMN
TSCA Experimental Release Applications (TERA)
6300-07
Bio Tech
Test Marketing Exemptions (TME)
7710-25
PMN
Tier 1 Exemptions
63007-07
BioTech
Tier II Exemptions
6300-07
BioTech
ICR Summary of Burden
Total Request
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
4,243
4,243
0
0
0
0
Annual Time Burden (Hours)
129,367
129,367
0
0
0
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:
Annual Cost to Federal Government:
$26,697,996
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:
Katherine Sleasman 202 564-7716 sleasman.katherine@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:
12/31/2025
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