Prescription Drug Marketing: Administrative Procedures, Policies, and Requirements

Forms and Documents

Forms and supporting documents for this ICR

Document	Type	Status	Availability
Form 3911 Drug Notification	Form	Modified	Available
Form 3911 Prescription Drug Marketing: Reporting	Form	Modified	Missing upstream
0435 PDMA 83-C to use Form FDA 3911 FEB 2025.docx	Justification for No Material/Nonsubstantive Change	Uploaded 2025-02-25	Available
0435 PDMA 83-C to use Form FDA 3911 FEB 2025.docx	Justification for No Material/Nonsubstantive Change	Uploaded 2025-02-25	Available
0435 PDMA SSA Ext 2024 FDA amended 1-17-25.docx	Supporting Statement A	Uploaded 2025-01-17	Available
0435 PDMA SSA Ext 2024 FDA amended 1-17-25.docx	Supporting Statement A	Uploaded 2025-01-17	Repair queued

IC Document Collections

Information collection document groups

IC ID	Collection	Type	Status	Form
43602	Prescription Drug Marketing: Reporting	Form	Modified	Drug Notification
43602	Prescription Drug Marketing: Reporting	Form	Modified
43602	Prescription Drug Marketing: Reporting	Instruction	Modified
190489	Prescription Drug Marketing: Recordkeeping		Unchanged

ICR Details

OMB Control No: 0910-0435	ICR Reference No: 202502-0910-009
Status: Active	Previous ICR Reference No: 202403-0910-010
Agency/Subagency: HHS/FDA	Agency Tracking No: CDER
Title: Prescription Drug Marketing: Administrative Procedures, Policies, and Requirements
Type of Information Collection: No material or nonsubstantive change to a currently approved collection	Common Form ICR:  No
Type of Review Request: Regular
OIRA Conclusion Action: Approved without change	Conclusion Date: 06/06/2025
Retrieve Notice of Action (NOA)	Date Received in OIRA: 03/31/2025
Terms of Clearance: Terms continue: Approved consistent with the understanding that, upon finalization of any agency rulemaking amending 21 CFR Part 203 (see RIN 0910-AH56), FDA will submit a request to revise the information collection accordingly. Furthermore, within the next 2 years, FDA will seek comment specifically on the accuracy of the change in burden estimate in this collection as explained below: Because current implementation of requirements under the Drug Supply Chain Security Act (currently approved in OMB control no. 0910-0806) apply to manufacturers, wholesalers, and dispensers as well as distributers, we have considered that current recordkeeping requirements for drug samples under 21 CFR part 203 may apply to more respondents. To account for this activity, we increased the number of responses and hours per each of the 140 pharmaceutical companies identified in Row 3 of Table 2 in Q-12 above (“§§ 203.30 – 203.39; documentation regarding sample distribution”), and have included it with the other recordkeeping elements.

table that charts list comparision

	Inventory as of this Action	Requested	Previously Approved
Expiration Date	02/29/2028	02/29/2028	02/29/2028
Responses	6,865,417	0	6,865,417
Time Burden (Hours)	577,572	0	577,572
Cost Burden (Dollars)	0	0	0

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Abstract: This information collection supports implementation of the Prescription Drug Marketing Act and FDA regulations. The regulations are intended to protect the public against the threat of subpotent, adulterated, counterfeit, and misbranded drugs posed by the existence of drug diversion schemes and a drug diversion submarket, and the absence of appropriate controls over and creation and maintenance of appropriate records regarding the distribution of prescription drugs.

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Authorizing Statute(s): None

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:
	89 FR 3928	01/22/2024
30-day Notice:	Federal Register Citation:	Citation Date:
	89 FR 48431	06/06/2024
Did the Agency receive public comments on this ICR? Yes

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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
Prescription Drug Marketing: Recordkeeping
Prescription Drug Marketing: Reporting	3911	Drug Notification

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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	6,865,417	6,865,417	0	0	0	0
Annual Time Burden (Hours)	577,572	577,572	0	0	0	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: $1,008,807

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: 03/31/2025

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