Pharmaceutical Distribution Supply Chain

Forms and Documents

Forms and supporting documents for this ICR

Document	Type	Status	Availability
Form 3911 Drug Notification	Form	Modified	Available
Form 3911 Consultation/Terminations of notifications	Form	Modified	Repair queued
Form 3911 Drug Notifications	Form	Modified	Available
Form 3911 Reporting: Notifications to FDA	Form	Modified	Repair queued
0806 Drug Supply Chain SSA 2022 Ext.docx	Supporting Statement A	Uploaded 2022-01-26	Repair queued

IC Document Collections

Information collection document groups

IC ID	Collection	Type	Status	Form
248286	Waivers, Exemptions, Exceptions	Other-21 USC 360eee-1(a)(3)	New
218221	Illegitimate Products; termination of notification	Other-Agency Guidance	Modified
218217	Illegitimate Products: notifications to trading partners	Other-Agency Guidance	Modified
218214	Consultation/Terminations of notifications	Form	Modified	Drug Notification
218214	Consultation/Terminations of notifications	Form	Modified
218211	Reporting: Notifications to FDA	Form	Modified	Drug Notifications
218211	Reporting: Notifications to FDA	Form	Modified
218211	Reporting: Notifications to FDA	Other-21 USC 360eee-1	Modified

ICR Details

OMB Control No: 0910-0806	ICR Reference No: 202107-0910-010
Status: Historical Active	Previous ICR Reference No: 201812-0910-001
Agency/Subagency: HHS/FDA	Agency Tracking No: CDER
Title: Pharmaceutical Distribution Supply Chain
Type of Information Collection: Revision of a currently approved collection	Common Form ICR:  No
Type of Review Request: Regular
OIRA Conclusion Action: Approved without change	Conclusion Date: 02/28/2022
Retrieve Notice of Action (NOA)	Date Received in OIRA: 01/26/2022
Terms of Clearance:

table that charts list comparision

	Inventory as of this Action	Requested	Previously Approved
Expiration Date	02/28/2025	36 Months From Approved	02/28/2022
Responses	324,622	0	59,232
Time Burden (Hours)	1,974,932	0	12,086
Cost Burden (Dollars)	0	0	0

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Abstract: This information collection implements the Drug Supply Chain Security Act. Manufacturers, repackagers, wholesale distributors, and dispensers must: (1) Notify FDA when they have determined that a product in their possession or control is illegitimate or if a manufacturer when they determine that a product has a high risk of illegitimacy; (2) terminate such notifications after consultation with FDA; (3) notify certain immediate trading partners about an illegitimate product or if a manufacturer about a product with a high risk of illegitimacy; and (4) notify immediate trading partners when such notifications are terminated.

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Authorizing Statute(s): US Code: 21 USC 360eee Name of Law: Drug Supply Chain Security 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:
	86 FR 49538	09/03/2021
30-day Notice:	Federal Register Citation:	Citation Date:
	87 FR 1419	01/11/2022
Did the Agency receive public comments on this ICR? Yes

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Number of Information Collection (IC) in this ICR: 5

table that charts list of burden

IC Title	Form No.	Form Name
Consultation/Terminations of notifications	3911	Drug Notification
Illegitimate Products: notifications to trading partners
Illegitimate Products; termination of notification
Reporting: Notifications to FDA	3911	Drug Notifications
Waivers, Exemptions, Exceptions

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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	324,622	59,232	0	0	265,390	0
Annual Time Burden (Hours)	1,974,932	12,086	0	0	1,962,846	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: As a result of changes and adjustments, our estimated burden for the information collection reflects a cumulative increase since last OMB review and approval of 265,390 responses and 1,962,846 hours annually. We attribute this increase to a more recent evaluation of the information collection and informal communications with industry and other interested stakeholders regarding burden estimates.

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Annual Cost to Federal Government: $242,130

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.     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: 01/26/2022

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