Viruses, Serums, Toxins, and Analogous Products Suspension, Revocation or Termination of Biological Licenses or Permits

Forms and Documents

Forms and supporting documents for this ICR

Document	Type	Status	Availability
71 2009 0318.xls	Supplementary Document	Uploaded 2010-03-03	Available
2009 ss 0318.doc	Supporting Statement A	Uploaded 2010-03-10	Available
79 2009 0318.xls	Supplementary Document	Uploaded 2010-03-03	Available

IC Document Collections

Information collection document groups

IC ID	Collection	Type	Status	Form
178880	Viruses, Serums, Toxins, and Analogous Products; Suspension, Revocation, or Termination of Biological Licenses or Permittes, Individuals and Households		Removed
178879	Viruses, Serums, Toxins, and Analogous Products Suspension, Revocation, or Termination of Biological Licenses or Permittes, Private Sector		Modified

ICR Details

OMB Control No: 0579-0318	ICR Reference No: 201003-0579-001
Status: Historical Inactive	Previous ICR Reference No: 200803-0579-002
Agency/Subagency: USDA/APHIS	Agency Tracking No:
Title: Viruses, Serums, Toxins, and Analogous Products Suspension, Revocation or Termination of Biological Licenses or Permits
Type of Information Collection: Extension without change of a currently approved collection	Common Form ICR:  No
Type of Review Request: Regular
OIRA Conclusion Action: Improperly submitted and continue	Conclusion Date: 05/05/2010
	Date Received in OIRA: 03/24/2010
Terms of Clearance: In accordance with 5 CFR 1320, this collection has been improperly submitted. In Question 15 of the supporting statement, APHIS states, "The number of respondents has decreased from 60 to 55 respondents. This is because APHIS is no longer counting 5 of the respondents twice. There is no change in burden, merely a bookkeeping change to consolidate IC's." OMB notes that the Agency did not enter any change to respondents or burden hours into ROCIS and that the collection is listed as an extension. Please resubmit this collection for consideration when the supporting statement has been corrected to accurately reflect this request for approval.

table that charts list comparision

	Inventory as of this Action	Requested	Previously Approved
Expiration Date	03/31/2010	36 Months From Approved	09/30/2010
Responses	60	0	60
Time Burden (Hours)	106	0	106
Cost Burden (Dollars)	0	0	0

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Abstract: The purpose of this collection is to collect information that will assist APHIS in its efforts to prevent biological products from harming animals, the public, and the environment.

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Authorizing Statute(s): US Code: 21 USC 117 Name of Law: Animal Industry Act of 1884
  

Citations for New Statutory Requirements: None

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Associated Rulemaking Information
RIN:	Stage of Rulemaking:	Federal Register Citation:	Date:
0579-AC29	Final or interim final rulemaking	72 FR 68	04/10/2007

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Federal Register Notices & Comments
60-day Notice:	Federal Register Citation:	Citation Date:
	74 FR 151	08/07/2009
Did the Agency receive public comments on this ICR? Yes

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

table that charts list of burden

IC Title	Form No.	Form Name
Viruses, Serums, Toxins, and Analogous Products Suspension, Revocation, or Termination of Biological Licenses or Permittes, Private Sector
Viruses, Serums, Toxins, and Analogous Products; Suspension, Revocation, or Termination of Biological Licenses or Permittes, Individuals and Households

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Burden increases because of Program Change due to Agency Discretion: Yes

Burden Increase Due to: Miscellaneous Actions

Burden decreases because of Program Change due to Agency Discretion: Yes

Burden Reduction Due to: Miscellaneous Actions

Short Statement: The number of respondents has decreased from 60 to 55 respondents. This is because APHIS is no longer counting 5 of the respondents twice. There is no change in burden, merely a bookkeeping change to consolidate IC's.

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Annual Cost to Federal Government: $5,632

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]? Uncollected

Is this ICR related to the Dodd-Frank Wall Street Reform and Consumer Protection Act, [Pub. L. 111-203]? Uncollected

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: 03/24/2010

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