[CPR] Possession, Use, and Transfer of Select Agents and Toxins (42 CFR 73)

Forms and Documents

Forms and supporting documents for this ICR

Document	Type	Status	Availability
Form 0920-0576 Administrative Review	Form	Modified	Available
Form 0920-0576 Administrative Review	Form	Modified	Repair queued
Form APHIS/CDC FORM 3 INCIDENT FORM TO REPORT POTENTIAL THEFT, LOSS, RELEASE, OR OCCUPATIONAL EXPOSURE	Form and Instruction	Modified	Available
Form APHIS/CDC FORM 3 Incident Form to Report Potential Theft, Loss, Release, or Occpational Exposure (APHIS/CDC Form 3)	Form and Instruction	Modified	Repair queued
Form 0920-0576 Records	Form	Modified	Available
Form 0920-0576 Records	Form	Modified	Repair queued
Form APHIS/CDC Form 2 Request to Transfer Select Agents and Toxins	Form and Instruction	Modified	Available
Form APHIS/CDC Form 2 Request to Transfer Select Agents and Toxins (APHIS/CDC Form 2)	Form and Instruction	Modified	Repair queued
Form 0920-0576 Training	Form	Modified	Available
Form 0920-0576 Training	Form	Modified	Repair queued
Form 0920-0576 Incident Response Plan	Form	Modified	Available
Form 0920-0576 Incident Response Plan	Form	Modified	Repair queued
Form 0920-0576 Request Regarding Restricted Experiment	Form	Modified	Available
Form 0920-0576 Request Regarding a Restricted Experiment	Form	Modified	Repair queued
Form 0920-0576 Biosafety Plan	Form	Modified	Available
Form 0920-0576 Biosafety Plan	Form	Modified	Repair queued
Form 0920-0576 Secuity Plan	Form	Modified	Available
Form 0920-0576 Security Plan	Form	Modified	Repair queued
Form 0920-0576 Request for Expedited Review	Form	Modified	Available
Form 0920-0576 Request for Expedited Review	Form	Modified	Repair queued
Form 0920-0576 Documentation of self-inspection	Form	Modified	Available
Form 0920-0576 Documentation of Self-Inspection	Form	Modified	Repair queued
Form 0920-0576 Amendment to Registration	Form	Modified	Available
Form 0920-0576 Amendment to a Certificate of Registration	Form	Modified	Repair queued
Form APHIS/CDC FORM 1 Application for Registration for Possession, Use, and Transfer of Select Agents and Toxins	Form	Modified	Available
Form APHIS/CDC FORM 1 Application for Registration (APHIS/CDC Form 1)	Form	Modified	Repair queued
Form Form 5 Request for Exemption	Form	Modified	Available
Form Form 5 Request for Exemption of Select Agent Agent and Toxin for an Investigational Product (APHIS/CDC Form 5)	Form	Modified	Repair queued
Form APHIS/CDC Form 4 ( Reporting the Identification of a Select Agent or Toxin from a Clinical/Diagnostic Specimen	Form and Instruction	Modified	Available
Form APHIS/CDC Form 4 ( Reporting the Identification of a Select Agent or Toxin from a Clinical/Diagnostic Specimen (APHIS/CDC Form 4A)	Form and Instruction	Modified	Repair queued
Form 0920-0576 Request for Exclusions	Form	Modified	Available
Form 0920-0576 Request for Exclusions	Form	Modified	Repair queued
Attachment 20 - HSR Determination.pdf	Supplementary Document	Uploaded 2024-01-10	Repair queued
Attachment 3 - eFSAP SORN_2020-10-27.pdf	Supplementary Document	Uploaded 2024-01-10	Repair queued
Attachment 2 - 60-Day FRN_20231109.pdf	Supplementary Document	Uploaded 2024-01-10	Repair queued
Attachment 1 - 2017_FSAP-USDA-FinalRule.pdf	Supplementary Document	Uploaded 2024-01-10	Repair queued
Attachment 1 - 2017_FSAP-CDC-FinalRule.pdf	Supplementary Document	Uploaded 2024-01-10	Repair queued
0920-0576-2023-SSB.docx	Supporting Statement B	Uploaded 2024-01-10	Repair queued
0920-0576-2023-SSA_final.docx	Supporting Statement A	Uploaded 2024-01-10	Repair queued

IC Document Collections

Information collection document groups

IC ID	Collection	Type	Status	Form
217521	Administrative Review	Form	Modified	Administrative Review
217521	Administrative Review	Form	Modified
217520	Incident Form to Report Potential Theft, Loss, Release, or Occpational Exposure (APHIS/CDC Form 3)	Form and Instruction	Modified	INCIDENT FORM TO REPORT POTENTIAL THEFT, LOSS, RELEASE, OR OCCUPATIONAL EXPOSURE
217520	Incident Form to Report Potential Theft, Loss, Release, or Occpational Exposure (APHIS/CDC Form 3)	Form and Instruction	Modified
217519	Records	Form	Modified	Records
217519	Records	Form	Modified
217518	Request to Transfer Select Agents and Toxins (APHIS/CDC Form 2)	Form and Instruction	Modified	Request to Transfer Select Agents and Toxins
217518	Request to Transfer Select Agents and Toxins (APHIS/CDC Form 2)	Form and Instruction	Modified
217517	Training	Form	Modified	Training
217517	Training	Form	Modified
217516	Incident Response Plan	Form	Modified	Incident Response Plan
217516	Incident Response Plan	Form	Modified
217515	Request Regarding a Restricted Experiment	Form	Modified	Request Regarding Restricted Experiment
217515	Request Regarding a Restricted Experiment	Form	Modified
217514	Biosafety Plan	Form	Modified	Biosafety Plan
217514	Biosafety Plan	Form	Modified
217512	Security Plan	Form	Modified	Secuity Plan
217512	Security Plan	Form	Modified
217511	Request for Expedited Review	Form	Modified	Request for Expedited Review
217511	Request for Expedited Review	Form	Modified
217510	Documentation of Self-Inspection	Form	Modified	Documentation of self-inspection
217510	Documentation of Self-Inspection	Form	Modified
217509	Amendment to a Certificate of Registration	Form	Modified	Amendment to Registration
217509	Amendment to a Certificate of Registration	Form	Modified
217508	Application for Registration (APHIS/CDC Form 1)	Form	Modified	Application for Registration for Possession, Use, and Transfer of Select Agents and Toxins
217508	Application for Registration (APHIS/CDC Form 1)	Form	Modified
217507	Request for Exemption of Select Agent Agent and Toxin for an Investigational Product (APHIS/CDC Form 5)	Form	Modified	Request for Exemption
217507	Request for Exemption of Select Agent Agent and Toxin for an Investigational Product (APHIS/CDC Form 5)	Form	Modified
217505	Reporting the Identification of a Select Agent or Toxin from a Clinical/Diagnostic Specimen (APHIS/CDC Form 4A)	Form and Instruction	Modified	Reporting the Identification of a Select Agent or Toxin from a Clinical/Diagnostic Specimen
217505	Reporting the Identification of a Select Agent or Toxin from a Clinical/Diagnostic Specimen (APHIS/CDC Form 4A)	Form and Instruction	Modified
217504	Request for Exclusions	Form	Modified	Request for Exclusions
217504	Request for Exclusions	Form	Modified

ICR Details

OMB Control No: 0920-0576	ICR Reference No: 202312-0920-005
Status: Active	Previous ICR Reference No: 202302-0920-015
Agency/Subagency: HHS/CDC	Agency Tracking No: 0920-0576
Title: [CPR] Possession, Use, and Transfer of Select Agents and Toxins (42 CFR 73)
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: 02/25/2024
Retrieve Notice of Action (NOA)	Date Received in OIRA: 01/17/2024
Terms of Clearance: CDC and USDA will consider updates to this package in accordance with any updates to the existing regulations. Previous terms continue: USDA and CDC will carefully monitor the usage of this system and update this package accordingly.

table that charts list comparision

	Inventory as of this Action	Requested	Previously Approved
Expiration Date	02/28/2027	36 Months From Approved	02/29/2024
Responses	3,482	0	4,453
Time Burden (Hours)	3,504	0	4,467
Cost Burden (Dollars)	0	0	0

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Abstract: The Centers for Disease Control and Prevention (CDC) collects information under 42CFR Part 73, with the purpose of ensuring select agents or toxins are managed appropriately to prevent any threats to human health or safety. The program changes in this requested extension are primarily changes to the forms to clarify instructions, correct editorial errors from previous submissions, and reformat the structure of the forms based on the day-to-day processing of these forms. There is a reduction in burden due to the decrease in the number of respondents.

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Authorizing Statute(s): PL: Pub.L. 107 - 188 Subtitle A Name of Law: Public Health Security and Bioterrorism Preparedness and Response Act of 2002
  

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:
	88 FR 55457	08/15/2023
30-day Notice:	Federal Register Citation:	Citation Date:
	89 FR 2615	01/16/2024
Did the Agency receive public comments on this ICR? No

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Number of Information Collection (IC) in this ICR: 16

table that charts list of burden

IC Title	Form No.	Form Name
Administrative Review	0920-0576	Administrative Review
Amendment to a Certificate of Registration	0920-0576	Amendment to Registration
Application for Registration (APHIS/CDC Form 1)	APHIS/CDC FORM 1	Application for Registration for Possession, Use, and Transfer of Select Agents and Toxins
Biosafety Plan	0920-0576	Biosafety Plan
Documentation of Self-Inspection	0920-0576	Documentation of self-inspection
Incident Form to Report Potential Theft, Loss, Release, or Occpational Exposure (APHIS/CDC Form 3)	APHIS/CDC FORM 3	INCIDENT FORM TO REPORT POTENTIAL THEFT, LOSS, RELEASE, OR OCCUPATIONAL EXPOSURE
Incident Response Plan	0920-0576	Incident Response Plan
Records	0920-0576	Records
Reporting the Identification of a Select Agent or Toxin from a Clinical/Diagnostic Specimen (APHIS/CDC Form 4A)	APHIS/CDC Form 4 (A, B, C)	Reporting the Identification of a Select Agent or Toxin from a Clinical/Diagnostic Specimen
Request Regarding a Restricted Experiment	0920-0576	Request Regarding Restricted Experiment
Request for Exclusions	0920-0576	Request for Exclusions
Request for Exemption of Select Agent Agent and Toxin for an Investigational Product (APHIS/CDC Form 5)	Form 5	Request for Exemption
Request for Expedited Review	0920-0576	Request for Expedited Review
Request to Transfer Select Agents and Toxins (APHIS/CDC Form 2)	APHIS/CDC Form 2	Request to Transfer Select Agents and Toxins
Security Plan	0920-0576	Secuity Plan
Training	0920-0576	Training

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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	3,482	4,453	0	-971	0	0
Annual Time Burden (Hours)	3,504	4,467	0	-963	0	0
Annual Cost Burden (Dollars)	0	0	0	0	0	0

Burden increases because of Program Change due to Agency Discretion: Yes

Burden Increase Due to: Miscellaneous Actions

Burden decreases because of Program Change due to Agency Discretion: Yes

Burden Reduction Due to: Miscellaneous Actions

Short Statement: There is a reduction in the estimate of respondents.

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Annual Cost to Federal Government: $19,274,049

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.     Yes

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.     Yes

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: 01/17/2024

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