Drug Supply Chain Security Act (DSCSA) Pilot Progam

Forms and Documents

Forms and supporting documents for this ICR

Document	Type	Status	Availability
DSCSA Pilot Project SSA 2018.pdf	Supporting Statement A	Uploaded 2018-08-10	Available

IC Document Collections

Information collection document groups

IC ID	Collection	Type	Status	Form
232655	DSCSA Pilot: Third Party Disclosure		New
232654	DSCSA Pilot: Recordkeeping		New
232652	DSCSA Pilot: Reporting		New

ICR Details

OMB Control No: 0910-0859	ICR Reference No: 201808-0910-006
Status: Active	Previous ICR Reference No:
Agency/Subagency: HHS/FDA	Agency Tracking No: CDER
Title: Drug Supply Chain Security Act (DSCSA) Pilot Progam
Type of Information Collection: New collection (Request for a new OMB Control Number)	Common Form ICR:  No
Type of Review Request: Regular
OIRA Conclusion Action: Approved without change	Conclusion Date: 08/29/2018
	Date Received in OIRA: 08/10/2018
Terms of Clearance:

table that charts list comparision

	Inventory as of this Action	Requested	Previously Approved
Expiration Date	08/31/2021	36 Months From Approved
Responses	216	0	0
Time Burden (Hours)	2,157	0	0
Cost Burden (Dollars)	0	0	0

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Abstract: FDA will be establishing the Drug Supply Chain Security Act (DSCSA) (Title II of Pub. L. 113-54) Pilot Project Program to implement section 582(j) of the Federal Food, Drug, and Cosmetic Act (the FD&C Act) (21 U.S.C. 360eee-1). This program will assist the development of the interoperable electronic system established by 2023.

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Authorizing Statute(s): PL: Pub.L. 113 - 54 Title II - Drug Supply Chain Name of Law: Drug Quality and Security Act
   US Code: 21 USC 301 et seq. Name of Law: Federal Food, Drug, and Cosmetic Act
  

Citations for New Statutory Requirements: PL: Pub.L. 113 - 54 Title II; Drug Security Chain Name of Law: Drug Quality and Security Act

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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:
	82 FR 33497	07/20/2017
30-day Notice:	Federal Register Citation:	Citation Date:
	83 FR 22085	05/11/2018
Did the Agency receive public comments on this ICR? Yes

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Number of Information Collection (IC) in this ICR: 3

table that charts list of burden

IC Title	Form No.	Form Name
DSCSA Pilot: Reporting
DSCSA Pilot: Recordkeeping
DSCSA Pilot: Third Party Disclosure

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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	216	0	216	0	0	0
Annual Time Burden (Hours)	2,157	0	2,157	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: This is a new information collection.

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Annual Cost to Federal Government: $360,250

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? 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: 08/10/2018

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