Food Additive Petitions, 21 CFR Part 571, Center for Veterinary Medicine

Forms and Documents

Document	Type	Status	Availability
0546 ss 4-5-2013.doc	Supporting Statement A	Uploaded 2013-04-05	Repair queued

IC Document Collections

IC ID	Collection	Type	Status	Form
6266	Moderate Category - Non-complex Food Additive Petitions		Modified
206417	Complex category - Investigational Food Additive Files		New
206416	Moderate category - Investigational Food Additive Files		New
191904	Amendment of Petitions		Modified
191903	Complex Category- Complex Food Additive Petitions		Modified

ICR Details

OMB Control No: 0910-0546	ICR Reference No: 201304-0910-002
Status: Historical Active	Previous ICR Reference No: 201001-0910-016
Agency/Subagency: HHS/FDA	Agency Tracking No: 19200
Title: Food Additive Petitions, 21 CFR Part 571, Center for Veterinary Medicine
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: 05/23/2013
	Date Received in OIRA: 04/09/2013
Terms of Clearance:

	Inventory as of this Action	Requested	Previously Approved
Expiration Date	05/31/2016	36 Months From Approved	05/31/2013
Responses	19	0	6
Time Burden (Hours)	51,700	0	18,200
Cost Burden (Dollars)	0	0	0

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Abstract: A food additive shall be deemed to be unsafe unless its use is permitted by a regulation which prescribes the condition(s) under which it may safely be used, or unless it is exempted by regulation for investigational use. Therefore, certain information must be submitted by a petition in order to establish the safety of a food additive and to secure the issuance of a regulation permitting its use in animal food.

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Authorizing Statute(s): US Code: 21 USC 409(a) Name of Law: Federal Food, Drug and Cosmetic 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:
	77 FR 67655	11/13/2012
30-day Notice:	Federal Register Citation:	Citation Date:
	78 FR 20661	04/05/2013
Did the Agency receive public comments on this ICR? No

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

IC Title	Form No.	Form Name
Moderate Category - Non-complex Food Additive Petitions
Complex Category- Complex Food Additive Petitions
Amendment of Petitions
Moderate category - Investigational Food Additive Files
Complex category - Investigational Food Additive Files

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ICR Summary 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	19	6	0	0	13	0
Annual Time Burden (Hours)	51,700	18,200	0	0	33,500	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: $42,660

Does this IC contain surveys, censuses, or employ statistical methods? No

Is the Supporting Statement intended to be a Privacy Impact Assessment required by the E-Government Act of 2002? 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: 04/09/2013

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