Designation of New Animal Drugs for Minor Use or Minor Species (MUMS) - Final Rule

Forms and Documents

Document Name	Status
0605 MUMS SS 2013.doc Supporting Statement A	2013-12-11

IC Document Collections

IC ID	Document Title	Status
181664	Designation of New Animal Drugs for Minor Use and MInor Species ( MUMS)	Modified

ICR Details

OMB Control No: 0910-0605	ICR Reference No: 201312-0910-004
Status: Historical Active	Previous ICR Reference No: 201009-0910-009
Agency/Subagency: HHS/FDA	Agency Tracking No: 21074
Title: Designation of New Animal Drugs for Minor Use or Minor Species (MUMS) - Final Rule
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: 02/07/2014
	Date Received in OIRA: 12/11/2013
Terms of Clearance:

	Inventory as of this Action	Requested	Previously Approved
Expiration Date	02/28/2017	36 Months From Approved	02/28/2014
Responses	157	0	157
Time Burden (Hours)	1,362	0	1,362
Cost Burden (Dollars)	0	0	0

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Abstract: The Minor Use and Minor Species Animal Health Act of 2004 (MUMS Act) provides incentives designed to help pharmaceutical companies overcome the financial burdens they face in providing limited-demand animal drugs. These incentives are only available to sponsors whose drugs are designated "MUMS" by FDA. Respondents to this collection, therefore, are sponsors of animal drugs used for minor animal species as well as uncommon diseases in major animal species who wish to obtain a MUMS designation for their products. Participation in the MUMS program is optional, however respondents must report certain information to the agency to obtain benefits offered by the MUMS program.

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Authorizing Statute(s): US Code: 21 USC 301 Name of Law: null
  

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:
	78 FR 39734	07/02/2013
30-day Notice:	Federal Register Citation:	Citation Date:
	78 FR 71623	11/29/2013
Did the Agency receive public comments on this ICR? No

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Number of Information Collection (IC) in this ICR: 1

IC Title	Form No.	Form Name
Designation of New Animal Drugs for Minor Use and MInor Species ( MUMS)

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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	157	157	0	0	0	0
Annual Time Burden (Hours)	1,362	1,362	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: $30,375

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: 12/11/2013

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