Consolidation of Certain Reporting and Recordkeeping under Section 8 of the Toxic Substances Control Act (TSCA) (Renewal)

Forms and Documents

Document Name	Status
Form 9600-07 Chemical Specific Rules TSCA section 8(a) Form and Instruction	Modified
Form 9600-032 Health and Safety Data Reporting, Submission of Lists and Copies of Health and Safety Studies TSCA section 8(d) Form and Instruction	Modified
Form 7710-35 TSCA 8a Preliminary Assessment Information Rule (PAIR) Form and Instruction	Modified
2703.02, Attachment, G Consultation_Responses.pdf Supplementary Document	2025-11-28
2703.02, Attachment F, Consultation.pdf Supplementary Document	2025-11-28
2703ss02.docx Supporting Statement A	2025-11-28

IC Document Collections

IC ID	Document Title	Status
255057	Chemical Specific Rules TSCA section 8(a) Form and Instruction	Modified
255049	Health and Safety Data Reporting, Submission of Lists and Copies of Health and Safety Studies TSCA section 8(d) Form and Instruction	Modified
255045	TSCA 8a Preliminary Assessment Information Rule (PAIR) Form and Instruction	Modified
255041	Allegations of Significant Adverse Reactions to Human Health or the Environment TSCA section 8(c)	Unchanged

ICR Details

OMB Control No: 2070-0224	ICR Reference No: 202511-2070-001
Status: Received in OIRA	Previous ICR Reference No: 202208-2070-001
Agency/Subagency: EPA/OCSPP	Agency Tracking No: 2703.02
Title: Consolidation of Certain Reporting and Recordkeeping under Section 8 of the Toxic Substances Control Act (TSCA) (Renewal)
Type of Information Collection: Revision of a currently approved collection	Common Form ICR:  No
Type of Review Request: Regular	Date Submitted to OIRA: 11/28/2025

	Requested	Previously Approved
Expiration Date	36 Months From Approved	11/30/2025
Responses	147,429	141,784
Time Burden (Hours)	106,523	59,855
Cost Burden (Dollars)	0	0

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Abstract: This consolidated ICR involves reporting and recordkeeping activities established under TSCA section 8 for chemical substances. Although imposed for a specific chemical substance, the activities are already established and only vary based on the specific authority under TSCA section 8 and the need for the information for that chemical. EPA is consolidating these ICRs to streamline the presentation of the paperwork burden estimates for these various activities, which will in turn facilitate and reduce the administrative burden for both the public reviewers and the Agency in terms of reviewing and updating the ICR every three (3) years as required by the Paperwork Reduction Act (PRA), 44 U.S.C. 3501 et seq., as well as allow for a better assessment of the paperwork burden and costs associated with reporting and recordkeeping activities established under TSCA section 8 for specific chemical substances. This information collection request (ICR) covers reporting and recordkeeping requirements imposed under the authorities in section 8 of the Toxic Substances Control Act (TSCA), 15 U.S.C. 2607, for persons who manufacture (the term manufacture includes import under TSCA)(Attachment 1) or process chemical substances, mixtures, or categories, or distribute them in commerce. The purpose of the information collection activities is to collect data that will help the Agency evaluate the potential for human health and environmental risks that may be caused by the manufacture, processing, and distribution in commerce of chemical substances, mixtures, or categories. This ICR addresses the following four (4) types of information collections (ICs) required by TSCA section 8 and identifies the persons required to keep records and report such information. The ICs are numbered to facilitate the presentation in the ICR and link to supporting information; and the numbering is not otherwise intended to convey any sequencing or prioritization.

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Authorizing Statute(s): US Code: 15 USC 2607 Name of Law: Toxic Substances Control Act
  

Citations for New Statutory Requirements: None

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Associated Rulemaking Information
RIN:	Stage of Rulemaking:	Federal Register Citation:	Date:
	Not associated with rulemaking

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Federal Register Notices & Comments
60-day Notice:	Federal Register Citation:	Citation Date:
	90 FR 19715	05/09/2025
30-day Notice:	Federal Register Citation:	Citation Date:
	90 FR 52381	11/20/2025
Did the Agency receive public comments on this ICR? Yes

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Number of Information Collection (IC) in this ICR: 4

IC Title	Form No.	Form Name
Allegations of Significant Adverse Reactions to Human Health or the Environment TSCA section 8(c)
Chemical Specific Rules TSCA section 8(a)	9600-07, 7710-25, 7710-51	Nanortechnology ,   PMN ,   Dioxin/Furan
Health and Safety Data Reporting, Submission of Lists and Copies of Health and Safety Studies TSCA section 8(d)	9600-032	TSCA Section 8(d) Health and Safety Data Screenshots
TSCA 8a Preliminary Assessment Information Rule (PAIR)	7710-35, 7710-51, 9600-07	Manufacturer's Report - Preliminary Assessment Info ,   Dioxin/Furan Report Form and Instructions ,   EPA Form 9600-07 Nanotechnology

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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	147,429	141,784	0	0	5,645	0
Annual Time Burden (Hours)	106,523	59,855	0	0	46,668	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: This increase is due to the fact that this ICR is absorbing two previously independent collections (647 hours from OMB Control Numbers 2070-0194 and 2070-0222). This ICR renewal incorporates an increase in burden identified in a recent TSCA section 8(d) rulemaking, published on December 13, 2024 (89 FR 100756), which incorporated an updated burden estimate arising out of a requirement to report studies showing any measurable content of the subject chemicals in response to information provided by stakeholders. This increase in burden would apply only where the Agency, via the applicable regulations, requires reporting of studies at any measurable content. EPA does not anticipate promulgating 8(d) rules requiring such reporting in this ICR's renewal period. Thus, despite this increase in burden being incorporated into this ICR, any 8(d) rules promulgated during this renewal period will not reflect this increase in burden. These changes are program adjustments.

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Annual Cost to Federal Government: $525,858

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

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Common Form ICR:  No

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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: 11/28/2025

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