Pre-Manufacture Review Reporting and Exemption Requirements for New Chemical Substances and Significant New Use Reporting Requirements for Chemical Substances

Forms and Documents

Document Name	Status
Form EPA Form 7710-25 Pre-Manufacture Notifications Form and Instruction	Modified
Form ESA and Authorizat CDX Electronic Signature Form	Removed
Form EPA Form 7710-56 Notice of Commencement Form and Instruction	Modified
Form EPA Form 7710-25 Research and Development Exemption Form and Instruction	Modified
Form EPA Form 7710-25 Instant Photographic Film Articles Exemption Form and Instruction	Modified
Form EPA Form 7710-25 Polymer Exemption Post-Manufacture Annual Reports Form and Instruction	Modified
Form EPA Form 7710-25 Non-Testing Activities under Section 5(e) Consent Orders Form and Instruction	Modified
Form EPA Form 7710-25 Test Data Submissions under Section 5(e) Consent Orders Form and Instruction	Modified
Form EPA Form 7710-25 Bona Fide Intent Notifications (Bona Fides) Form and Instruction	Modified
Form EPA Form 6300-7 Tier I/Tier II Exemptions Form	Modified
Form EPA Form 6300-7 TSCA Experimental Release Applications (TERAs) Form	Modified
Form EPA Form 7710-25 Low Volume and Low Release/Low Exposure Exemptions (LVE/LoREX) Form and Instruction	Modified
Form EPA Form 7710-25 Test-Marketing Exemptions (TMEs) Form and Instruction	Modified
Form EPA Form Number 63 Microbial Commercial Activity Notices (MCANs) Form	Modified
Form EPA Form 7710-25 PMN-Related Significant New Use Notices (SNUNs) Form and Instruction	Modified
AttachmentJ.doc Supplementary Document	2011-10-12
AttachmentI.pdf Supplementary Document	2011-10-12
AttachmentH.pdf Supplementary Document	2011-10-12
AttachmentG2partII.pdf Supplementary Document	2011-10-12
AttachmentG1-partI.pdf Supplementary Document	2011-10-12
AttachmentF.doc Supplementary Document	2011-10-12
AttachmentE.doc Supplementary Document	2011-10-12
AttachmentD.doc Supplementary Document	2011-10-12
AttachmentC.doc Supplementary Document	2011-10-12
AttachmentA.doc Supplementary Document	2011-10-12
AttachmentB.doc Supplementary Document	2011-10-12
cdxguide.pdf Supplementary Document	2010-04-09
cdxhints.pdf Supplementary Document	2010-04-09
cdxguide.pdf Supplementary Document	2010-04-09
HelpfulHints.pdf Supplementary Document	2011-10-12
0574ss15.docx Supporting Statement A	2011-11-30

IC Document Collections

IC ID	Document Title	Status
24844	Pre-Manufacture Notifications Form and Instruction	Modified
192556	e-PMN Rule Familiarization	Removed
192555	Establishment of a Pay.gov account	Removed
192554	CDX Electronic Signature Form	Removed
192553	CDX Registration	Removed
183119	Notice of Commencement Form and Instruction	Modified
183118	Research and Development Exemption Form and Instruction	Modified
183117	Instant Photographic Film Articles Exemption Form and Instruction	Modified
183116	Polymer Exemption Post-Manufacture Annual Reports Form and Instruction	Modified
183115	Non-Testing Activities under Section 5(e) Consent Orders Form and Instruction	Modified
183114	Test Data Submissions under Section 5(e) Consent Orders Form and Instruction	Modified
183113	Bona Fide Intent Notifications (Bona Fides) Form and Instruction	Modified
183112	Tier I/Tier II Exemptions Form	Modified
183111	TSCA Experimental Release Applications (TERAs) Form	Modified
183110	Low Volume and Low Release/Low Exposure Exemptions (LVE/LoREX) Form and Instruction	Modified
183109	Test-Marketing Exemptions (TMEs) Form and Instruction	Modified
183108	Microbial Commercial Activity Notices (MCANs) Form	Modified
183107	PMN-Related Significant New Use Notices (SNUNs) Form and Instruction	Modified

ICR Details

OMB Control No: 2070-0012	ICR Reference No: 201112-2070-001
Status: Historical Active	Previous ICR Reference No: 201004-2070-002
Agency/Subagency: EPA/OCSPP	Agency Tracking No: 0574.15
Title: Pre-Manufacture Review Reporting and Exemption Requirements for New Chemical Substances and Significant New Use Reporting Requirements for Chemical Substances
Type of Information Collection: Extension without change of a currently approved collection	Common Form ICR:  No
Type of Review Request: Regular
OIRA Conclusion Action: Approved without change	Conclusion Date: 12/21/2012
	Date Received in OIRA: 12/07/2011
Terms of Clearance: In accordance with 5 CFR 1320, the information collection is approved for 3 years.

	Inventory as of this Action	Requested	Previously Approved
Expiration Date	12/31/2015	36 Months From Approved	12/31/2012
Responses	2,126	0	2,518
Time Burden (Hours)	117,163	0	117,512
Cost Burden (Dollars)	0	0	0

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Abstract: Section 5 of the Toxic Substances Control Act (TSCA) requires manufacturers and importers of new chemical substances to submit to EPA a notice of intent to manufacture or import a new chemical substance 90 days before manufacture or import begins. (Formerly accomplished via paper documents, but now done electronically!) EPA reviews the information contained in the notice to evaluate the health and environmental effects of the new chemical substance. On the basis of the review, EPA may take further regulatory action under TSCA, if warranted. If EPA takes no action within 90 days, the submitter is free to manufacture or import the new chemical substance without restriction. TSCA section 5 also authorizes EPA to issue Significant New Use Rules (SNURs). EPA uses this authority to take follow-up action on new or existing chemicals that may present an unreasonable risk to human health or the environment if used in a manner that may result in different and/or higher exposures of a chemical to humans or the environment. Once a use is determined to be a significant new use, persons must submit a notice to EPA 90 days before beginning manufacture, processing or importation of a chemical substance for that use. Such a notice allows EPA to receive and review information on such a use and, if necessary, regulate the use before it occurs. Finally, TSCA section 5 also permits applications for exemption from section 5 review under certain circumstances. An applicant must provide information sufficient for EPA to make a determination that the circumstances in question qualify for an exemption. In granting an exemption, EPA may impose appropriate restrictions. This information collection addresses the reporting and recordkeeping requirements associated with TSCA section 5.

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Authorizing Statute(s): US Code: 15 USC 2605 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:
	76 FR 46794	08/03/2011
30-day Notice:	Federal Register Citation:	Citation Date:
	76 FR 76403	12/07/2011
Did the Agency receive public comments on this ICR? No

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Number of Information Collection (IC) in this ICR: 14

IC Title	Form No.	Form Name
PMN-Related Significant New Use Notices (SNUNs)	EPA Form 7710-25	Premanufacture Notice
Microbial Commercial Activity Notices (MCANs)	EPA Form Number 6300-07	EPA Biotech Form
Test-Marketing Exemptions (TMEs)	EPA Form 7710-25	Premanufacture Notice
Low Volume and Low Release/Low Exposure Exemptions (LVE/LoREX)	EPA Form 7710-25	Premanufacture Notice
TSCA Experimental Release Applications (TERAs)	EPA Form 6300-7	EPA Biotech Form
Tier I/Tier II Exemptions	EPA Form 6300-7	EPA Biotech Form
Bona Fide Intent Notifications (Bona Fides)	EPA Form 7710-25	Premanufacture Notice
Test Data Submissions under Section 5(e) Consent Orders	EPA Form 7710-25	Premanufacture Notice
Non-Testing Activities under Section 5(e) Consent Orders	EPA Form 7710-25	Premanufacture Notice
Polymer Exemption Post-Manufacture Annual Reports	EPA Form 7710-25	Premanufacture Notice
Instant Photographic Film Articles Exemption	EPA Form 7710-25	Premanufacture Notice
Research and Development Exemption	EPA Form 7710-25	Premanufacture Notice
Notice of Commencement	EPA Form 7710-56	Notice of Commencement of Manufacture or Import
CDX Registration
CDX Electronic Signature	ESA and Authorization Form 1, US EPA Electronic Signature Agreement, ESA and Authorization Form 2	Verification of Company Authorizing Official ,   US EPA Electronic Signature Agreement ,   Authorization And Verification For Section 5 Notice Support Submitter By Company Authorizing Official
Establishment of a Pay.gov account
e-PMN Rule Familiarization
Pre-Manufacture Notifications	EPA Form 7710-25	Premanufacture Notice

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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	2,126	2,518	0	0	-392	0
Annual Time Burden (Hours)	117,163	117,512	0	0	-349	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:

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Annual Cost to Federal Government: $6,397,518

Does this IC contain surveys, censuses, or employ statistical methods? No

Is the Supporting Statement intended to be a Privacy Impact Assessment required by the E-Government Act of 2002? 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? Uncollected

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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: 12/07/2011

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