National Electronic Injury Surveillance System (NEISS) and Follow-up Activities for Product Related Injuries

Forms and Documents

Forms and supporting documents for this ICR

Document	Type	Status	Availability
Form 182 Follow-Up Activities for Product-Related Injuries-Interviews	Form and Instruction	Modified	Available
Form OMB0029-PC-NEISS-S NEISS	Form and Instruction	Modified	Available
FY2020 C&R Manual.pdf	Supplementary Document	Uploaded 2020-03-11	Available
2020 NEISS AIP Coding Manual.pdf	Supplementary Document	Uploaded 2020-03-11	Available
2020 CPSC Only Non-Trauma Coding Manual.pdf	Supplementary Document	Uploaded 2020-03-11	Available
OMB0029_NEISS_Supporting_Statement_20200327.pdf	Supporting Statement B	Uploaded 2020-03-27	Available
OMB0029_NEISS_Supporting_Statement_20200327.pdf	Supporting Statement A	Uploaded 2020-03-27	Available
30 Day Notice 2019-27509.pdf	Supplementary Document	Uploaded 2019-12-23	Available
60 Day Notice CPSC-2009-0102-0007.pdf	Supplementary Document	Uploaded 2019-12-23	Available
Form 182 from 2011 Field Manual for Investigations.pdf	Supplementary Document	Uploaded 2013-07-18	Available
PIA_National Electronic Injury Surveillance System (NEISS).pdf	Supplementary Document	Uploaded 2010-03-31	Available
OMB(40)MedicalExaminerCoronerReport.pdf	Supplementary Document	Uploaded 2006-11-07	Available
OMB(38)HealthCareProfessional.pdf	Supplementary Document	Uploaded 2006-11-07	Available
OMB(37)FirePoliceInsuranceInvestigator.pdf	Supplementary Document	Uploaded 2006-11-07	Available

IC Document Collections

Information collection document groups

IC ID	Collection	Type	Status	Form
29149	Follow-Up Activities for Product-Related Injuries-Interviews	Form and Instruction	Modified
207798	NEISS	Form and Instruction	Modified

ICR Details

OMB Control No: 3041-0029	ICR Reference No: 201912-3041-001
Status: Active	Previous ICR Reference No: 201609-3041-002
Agency/Subagency: CPSC	Agency Tracking No:
Title: National Electronic Injury Surveillance System (NEISS) and Follow-up Activities for Product Related Injuries
Type of Information Collection: Revision of a currently approved collection	Common Form ICR:  No
Type of Review Request: Regular
OIRA Conclusion Action: Approved with change	Conclusion Date: 04/03/2020
	Date Received in OIRA: 12/23/2019
Terms of Clearance: When this ICR is renewed, CPSC should explain the results of the independent statistical assessment and changes made to the ICR in response to that assessment.

table that charts list comparision

	Inventory as of this Action	Requested	Previously Approved
Expiration Date	07/31/2022	36 Months From Approved	04/30/2020
Responses	728,144	0	741,853
Time Burden (Hours)	102,544	0	82,853
Cost Burden (Dollars)	0	0	0

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Abstract: Persons who have been injured in or who have witnessed safety- related incidents involving consumer products are an important source of safety information. The Commission uses information obtained from these persons and hospital emergency rooms to support activities to eliminate or reduce unreasonable risks of injury associated with consumer products.

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Authorizing Statute(s): US Code: 15 USC 2054 Name of Law: Consumer Product Safety 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:
	84 FR 53707	10/08/2019
30-day Notice:	Federal Register Citation:	Citation Date:
	84 FR 70157	12/20/2019
Did the Agency receive public comments on this ICR? No

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Number of Information Collection (IC) in this ICR: 2

table that charts list of burden

IC Title	Form No.	Form Name
NEISS	OMB0029-PC-NEISS-Screenshots	PC-NEISS
Follow-Up Activities for Product-Related Injuries-Interviews	182	Epidemiologic Investigation Report

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ICR Summary of Burden

table that charts list 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	728,144	741,853	0	0	-13,709	0
Annual Time Burden (Hours)	102,544	82,853	0	0	19,691	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: $5,400,000

Does this IC contain surveys, censuses, or employ statistical methods? Yes Part B of Supporting Statement

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? 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: 12/23/2019

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