Pet Event Tracking Network (PETNet)--State, Federal Cooperation to Prevent Spread of Pet Food Related Diseases

Forms and Documents

Document Name	Status
0680 PetNet Supporting Statement Part A 2014.docx Supporting Statement A	2014-02-28

IC Document Collections

IC ID	Document Title	Status
195930	PetNet Reporting Portal; FDA Form 3756 Other-Form and Portal Screen Shots	Modified

ICR Details

OMB Control No: 0910-0680	ICR Reference No: 201403-0910-001
Status: Historical Active	Previous ICR Reference No: 201101-0910-005
Agency/Subagency: HHS/FDA	Agency Tracking No: 21311
Title: Pet Event Tracking Network (PETNet)--State, Federal Cooperation to Prevent Spread of Pet Food Related Diseases
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: 05/16/2014
	Date Received in OIRA: 03/03/2014
Terms of Clearance:

	Inventory as of this Action	Requested	Previously Approved
Expiration Date	05/31/2017	36 Months From Approved	05/31/2014
Responses	200	0	500
Time Burden (Hours)	50	0	167
Cost Burden (Dollars)	0	0	0

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Abstract: The PETNet program will allow FDA and participating members to quickly and effectively exchange information about outbreaks of illness in both companion animals and livestock. FDA has worked closely with its Federal and State partners to develop the PETNet reporting portal, and believes that information collected under this program will serve an important function in protecting the public and animal health. Respondents to the collection are state and federal government officials who voluntary participate in the program.

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Authorizing Statute(s): US Code: 21 USC 342-343 Name of Law: Section 1002(b) of the FDA Amendments Act of 2007/FD&C 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:
	78 FR 52774	08/26/2013
30-day Notice:	Federal Register Citation:	Citation Date:
	79 FR 10529	02/25/2014
Did the Agency receive public comments on this ICR? Yes

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

IC Title	Form No.	Form Name
PetNet Reporting Portal; FDA Form 3756

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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	200	500	0	0	-300	0
Annual Time Burden (Hours)	50	167	0	0	-117	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 revision to a currently approved collection.

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Annual Cost to Federal Government: $105,211

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: 03/03/2014

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