[Federal Register Volume 76, Number 122 (Friday, June 24, 2011)]
[Notices]
[Pages 37057-37058]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2011-15888]


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DEPARTMENT OF AGRICULTURE

Animal and Plant Health Inspection Service

[Docket No. APHIS-2011-0061]


Notice of Request for Extension of Approval of an Information 
Collection; Virus-Serum-Toxin Act and Regulations

AGENCY: Animal and Plant Health Inspection Service, USDA.

ACTION: Extension of approval of an information collection; comment 
request.

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SUMMARY: In accordance with the Paperwork Reduction Act of 1995, this 
notice announces the Animal and Plant Health Inspection Service's 
intention to request an extension of approval of an information 
collection associated with the Virus-Serum-Toxin Act and regulations.

DATES: We will consider all comments that we receive on or before 
August 23, 2011.

ADDRESSES: You may submit comments by either of the following methods:
     Federal eRulemaking Portal: Go to http://www.regulations.gov/#!documentDetail;D=APHIS-2011-0061-0001.
     Postal Mail/Commercial Delivery: Send your comment to 
Docket No. APHIS-2011-0061, Regulatory Analysis and Development, PPD, 
APHIS, Station 3A-03.8, 4700 River Road Unit 118, Riverdale, MD 20737-
1238.
    Supporting documents and any comments we receive on this docket may 
be viewed at http://www.regulations.gov/#!docketDetail;D=APHIS-2011-
0061 or in our reading room, which is located in room 1141 of the USDA 
South Building, 14th Street and Independence Avenue, SW., Washington, 
DC. Normal reading room hours are 8 a.m. to 4:30 p.m., Monday through 
Friday, except holidays. To be sure someone is there to help you, 
please call (202) 690-2817 before coming.

FOR FURTHER INFORMATION CONTACT: For information on the Virus-Serum-
Toxin Act and regulations, contact Dr. Albert Morgan, Section Leader, 
Operational Support Staff, Center for Veterinary Biologics, VS, APHIS, 
4700 River Road Unit 148, Riverdale, MD 20737; (301) 734-8725. For 
copies of more detailed information on the information collection, 
contact Mrs. Celeste Sickles, APHIS' Information Collection 
Coordinator, at (301) 851-2908.

SUPPLEMENTARY INFORMATION:
    Title: Virus-Serum-Toxin Act and Regulations.
    OMB Number: 0579-0013.
    Type of Request: Extension of approval of an information 
collection.
    Abstract: Under the Virus-Serum-Toxin Act (21 U.S.C. 151-159), the 
Animal and Plant Health Inspection Service is authorized to promulgate 
regulations designed to prevent the importation, preparation, sale, or 
shipment of harmful veterinary biological products. These regulations 
are contained in title 9, Code of Federal Regulations, subchapter E, 
parts 102 to 124.
    Veterinary biological products include viruses, serums, toxins, and 
analogous products of natural or synthetic origin, such as vaccines, 
antitoxins, or the immunizing components of microorganisms intended for 
the diagnosis, treatment, or prevention of diseases in domestic 
animals.
    APHIS issues licenses to qualified establishments that produce 
veterinary biological products and issues permits to importers of such 
products. We also enforce requirements concerning production, 
packaging, labeling, and shipping of these products and set standards 
for the testing of these products.
    To help ensure that veterinary biological products used in the 
United States are pure, safe, potent, and effective, APHIS requires 
certain information collection activities, including establishment 
license applications, product license applications, product import 
permit applications, product and test report forms, and field study 
summaries.
    We are asking the Office of Management and Budget (OMB) to approve 
our use of these information collection activities for an additional 3 
years.
    The purpose of this notice is to solicit comments from the public 
(as well as affected agencies) concerning our information collection. 
These comments will help us:
    (1) Evaluate whether the collection of information is necessary for 
the proper performance of the functions of the Agency, including 
whether the information will have practical utility;
    (2) Evaluate the accuracy of our estimate of the burden of the 
collection of information, including the validity of the methodology 
and assumptions used;
    (3) Enhance the quality, utility, and clarity of the information to 
be collected; and
    (4) Minimize the burden of the collection of information on those 
who are to respond, through use, as appropriate, of automated, 
electronic, mechanical, and other collection technologies; e.g., 
permitting electronic submission of responses.
    Estimate of burden: The public reporting burden for this collection 
of information is estimated to average 3.42359 hours per response.
    Respondents: U.S. importers, exporters, and shippers of veterinary 
biological products; State veterinary authorities; and operators of 
establishments that produce or test veterinary biological products or 
that

[[Page 37058]]

engage in product research and development.
    Estimated annual number of respondents: 200.
    Estimated annual number of responses per respondent: 108.63.
    Estimated annual number of responses: 21,726.
    Estimated total annual burden on respondents: 74,381 hours. (Due to 
averaging, the total annual burden hours may not equal the product of 
the annual number of responses multiplied by the reporting burden per 
response.)
    All responses to this notice will be summarized and included in the 
request for OMB approval. All comments will also become a matter of 
public record.

    Done in Washington, DC, this 20th day of June 2011.
Kevin Shea,
Acting Administrator, Animal and Plant Health Inspection Service.
[FR Doc. 2011-15888 Filed 6-23-11; 8:45 am]
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