CDC/HRSA Advisory Committee on HIV and STD Prevention and Treatment, 23733-23734 [2012-9549]
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23733
Federal Register / Vol. 77, No. 77 / Friday, April 20, 2012 / Notices
reports on the physical examination of
herds, while § 1210.13 requires the
reporting of tuberculin testing of the
herds. In addition, the regulations in
part 1210 require that dairy farmers and
plants maintain pasteurization records
(§ 1210.15) and that each container of
milk or cream imported into the United
States bear a tag with the product type,
permit number, and shipper’s name and
address (§ 1210.22). Section 1210.20
requires that an application for a permit
to ship or transport milk or cream into
the United States be made by the actual
shipper. Section 1210.23 allows permits
to be granted based on certificates from
accredited officials.
FDA estimates the burden of this
collection of information as follows:
TABLE 1—ESTIMATED ANNUAL REPORTING BURDEN 1
Number of
responses per
respondent
Number of
respondents
Average burden
per response
Total hours
400
1.5
600
1
1
0.5
0.5
1
2
1
1
1
2
0.5
2
0.5
4
2
2
1
1
2
2
0.5
0.5
1
1
........................
........................
........................
..........................
607
21 CFR Section
Form No.
1210.11 ...............
FDA 1996/Sanitary inspection of
dairy farms.
FDA 1995/Physical examination of
cows.
FDA 1994/Tuberculin test ...............
FDA 1997/Sanitary inspections of
plants.
FDA 1993/Application for permit ....
FDA 1815/Permits granted on certificates.
2
200
1
.........................................................
Total annual
responses
1210.12 ...............
1210.13 ...............
1210.14 ...............
1210.20 ...............
1210.23 ...............
Total ............
1 There
are no capital costs or operating and maintenance costs associated with this collection of information.
TABLE 2—ESTIMATED ANNUAL RECORDKEEPING BURDEN 1
21 CFR Section
Number of
recordkeepers
Number of records
per recordkeeper
Total annual
records
Average burden
per recordkeeping
Total hours
1210.15 ..................................................
2
1
2
0.05
0.10
tkelley on DSK3SPTVN1PROD with NOTICES
1 There
are no capital costs or operating and maintenance costs associated with this collection of information.
The estimated number of respondents
and hours per response are based on
FDA’s experience with the import milk
permit program and the average number
of import milk permit holders over the
past 3 years. FDA estimates that two
respondents will submit approximately
200 Form FDA 1996 reports annually,
for a total of 600 responses. FDA
estimates the reporting burden to be 1.5
hours per response, for a total burden of
607 hours.
The Secretary of Health and Human
Services has the discretion to allow
Form FDA 1815, a duly certified
statement signed by an accredited
official of a foreign government, to be
submitted in lieu of Forms FDA 1994
and 1995. To date, Form FDA 1815 has
been submitted in lieu of these forms.
Because FDA has not received any
Forms FDA 1994 and 1995 in the last 3
years, the Agency estimates no more
than one will be submitted annually.
FDA estimates the reporting burden for
each to be 0.5 hours per response for a
total burden reporting burden of 0.5
hours each.
FDA estimates that two respondents
will submit one Form FDA 1997 report
annually, for a total of two responses.
FDA estimates the reporting burden to
be 2.0 hours per response, for a total
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burden of 4 hours. FDA estimates that
two respondents will submit one Form
FDA 1993 report annually, for a total of
two responses. FDA estimates the
reporting burden to be 0.5 hours per
response, for a total burden of 1 hour.
FDA estimates that two respondents
will submit one Form FDA 1815 report
annually, for a total of two responses.
FDA estimates the reporting burden to
be 0.5 hours per response, for a total
burden of 1 hour.
With regard to records maintenance,
FDA estimates that approximately two
recordkeepers will spend 0.05 hours
annually maintaining the additional
pasteurization records required by
§ 1210.15, for a total of 0.10 hours
annually.
No burden has been estimated for the
tagging requirement in § 1210.22
because the information on the tag is
either supplied by FDA (permit number)
or is disclosed to third parties as a usual
and customary part of the shipper’s
normal business activities (type of
product, shipper’s name and address).
Under 5 CFR 1320.3(c)(2), the public
disclosure of information originally
supplied by the Federal Government to
the recipient for the purpose of
disclosure to the public is not a
collection of information. Under 5 CFR
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1320.3(b)(2)), the time, effort, and
financial resources necessary to comply
with a collection of information are
excluded from the burden estimate if
the reporting, recordkeeping, or
disclosure activities needed to comply
are usual and customary because they
would occur in the normal course of
business activities.
Dated: April 16, 2012.
Leslie Kux,
Assistant Commissioner for Policy.
[FR Doc. 2012–9532 Filed 4–19–12; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
Health Resources and Services
Administration
CDC/HRSA Advisory Committee on
HIV and STD Prevention and Treatment
In accordance with section 10(a)(2) of
the Federal Advisory Committee Act
(Pub. L. 92–463), the Centers for Disease
Control and Prevention (CDC) and the
Health Resources and Services
E:\FR\FM\20APN1.SGM
20APN1
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Federal Register / Vol. 77, No. 77 / Friday, April 20, 2012 / Notices
Intent to Petition for Legal Custody for
Public Law 97–359 Amerasian.
Administration (HRSA) announce the
following meeting of the
aforementioned committee:
Times and Dates:
8 a.m.–5:30 p.m., May 8, 2012.
8 a.m.–3 p.m., May 9, 2012.
Place: The Westin Buckhead Atlanta, 3391
Peachtree Road, NE.,
Atlanta, Georgia, 30326, Telephone: (404)
365–0065.
Status: Open to the public, limited only by
the space available.
The meeting room will accommodate
approximately 100 people.
Purpose: This Committee is charged with
advising the Director, CDC and the
Administrator, HRSA, regarding activities
related to prevention and control of HIV/
AIDS and other STDs, the support of health
care services to persons living with HIV/
AIDS, and education of health professionals
and the public about HIV/AIDS and other
STDs.
Matters To Be Discussed: Agenda items
include: (1) Enhancing Hepatitis Prevention
Treatment and Care in the United States;
(2) Integrating HIV Prevention and Care
Data Systems; (3) External Peer Review of
CDC Youth HIV/STI Prevention and Sexual
Health Activities; (4) Preparing for the Ryan
White Reauthorization; and (5) CHAC
Workgroups Update.
Agenda items are subject to change as
priorities dictate.
Contact Person for More Information:
Margie Scott-Cseh, CDC, National Center for
HIV/AIDS, Viral Hepatitis, STD, and TB
Prevention, 1600 Clifton Road, NE., Mailstop
E–07, Atlanta, Georgia 30333, Telephone
(404) 639–8317.
The Director, Management Analysis and
Services Office, has been delegated the
authority to sign Federal Register Notices
pertaining to announcements of meetings and
other committee management activities, for
both the Centers for Disease Control and
Prevention and the Agency for Toxic
Substances and Disease Registry.
Dated: April 16, 2012.
Elaine L. Baker,
Director, Management Analysis and Services
Office, Centers for Disease Control and
Prevention.
[FR Doc. 2012–9549 Filed 4–19–12; 8:45 am]
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DEPARTMENT OF HOMELAND
SECURITY
tkelley on DSK3SPTVN1PROD with NOTICES
U.S. Citizenship and Immigration
Services
Agency Information Collection
Activities: Form I–361, Extension of a
Currently Approved Information
Collection; Comment Request
30-Day Notice of Information
Collection Under Review: Form I–361,
Affidavit of Financial Support and
ACTION:
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The Department of Homeland
Security, U.S. Citizenship and
Immigration Services (USCIS) will be
submitting the following information
collection request to the Office of
Management and Budget (OMB) for
review and clearance in accordance
with the Paperwork Reduction Act of
1995. The information collection notice
was previously published in the Federal
Register on February 16, 2012, at 77 FR
9259, allowing for a 60-day public
comment period. USCIS did not receive
any comments for this information
collection.
The purpose of this notice is to allow
an additional 30 days for public
comments. Comments are encouraged
and will be accepted until May 21,
2012. This process is conducted in
accordance with 5 CFR 1320.10.
Written comments and/or suggestions
regarding the item(s) contained in this
notice, especially regarding the
estimated public burden and associated
response time, should be directed to the
Department of Homeland Security
(DHS), and to the Office of Information
and Regulatory Affairs, Office of
Management and Budget (OMB), USCIS
Desk Officer. Comments may be
submitted to: USCIS, Chief Regulatory
Coordinator, Regulatory Coordination
Division, Office of Policy and Strategy,
Clearance Office, 20 Massachusetts
Avenue, Washington, DC 20529.
Comments may also be submitted to
DHS via facsimile to 202–272–0997 or
via email at uscisfrcomment@dhs.gov,
and to the OMB USCIS Desk Officer via
facsimile at 202–395–6974 or via email
at oira_submission@omb.eop.gov.
When submitting comments by email
please make sure to add OMB Control
Number 1615–0021 in the subject box.
Written comments and suggestions from
the public and affected agencies should
address one or more of the following
four points:
(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 the
agencies 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, including through the
use of appropriate automated,
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electronic, mechanical, or other
technological collection techniques or
other forms of information technology,
e.g., permitting electronic submission of
responses.
Overview of This Information
Collection
(1) Type of Information Collection:
Extension of a currently approved
information collection.
(2) Title of the Form/Collection:
Affidavit of Financial Support and
Intent to Petition for Legal Custody for
Public Law 97–359 Amerasian.
(3) Agency form number, if any, and
the applicable component of the
Department of Homeland Security
sponsoring the collection: Form I–361.
U.S. Citizenship and Immigration
Services.
(4) Affected public who will be asked
or required to respond, as well as a brief
abstract: Primary: Individuals and
households. The information on this
form is used in support of Form I–360
(Petition for Amerasian, Widow(er), or
Special Immigrant) to ensure financial
support for Public Law 97–359
Amerasian. The affidavit is used only to
sponsor individuals eligible for
immigration under Public Law 97–359.
(5) An estimate of the total number of
respondents and the amount of time
estimated for an average respondent to
respond: 50 responses at 30 minutes
(.50) per response.
(6) An estimate of the total public
burden (in hours) associated with the
collection: 25 annual burden hours.
If you have additional comments,
suggestions, or need a copy of the
information collection instrument,
please visit the USCIS Web site at:
https://www.regulations.gov/.
We may also be contacted at: USCIS,
Regulatory Coordination Division,
Office of Policy and Strategy, 20
Massachusetts Avenue NW.,
Washington, DC 20529, Telephone
number 202–272–1470.
Dated: April 16, 2012.
Laura Dawkins,
Acting Chief Regulatory Coordinator,
Regulatory Coordination Division, Office of
Policy and Strategy, U.S. Citizenship and
Immigration Services, Department of
Homeland Security.
[FR Doc. 2012–9616 Filed 4–19–12; 8:45 am]
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[Federal Register Volume 77, Number 77 (Friday, April 20, 2012)]
[Notices]
[Pages 23733-23734]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2012-9549]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
Health Resources and Services Administration
CDC/HRSA Advisory Committee on HIV and STD Prevention and
Treatment
In accordance with section 10(a)(2) of the Federal Advisory
Committee Act (Pub. L. 92-463), the Centers for Disease Control and
Prevention (CDC) and the Health Resources and Services
[[Page 23734]]
Administration (HRSA) announce the following meeting of the
aforementioned committee:
Times and Dates:
8 a.m.-5:30 p.m., May 8, 2012.
8 a.m.-3 p.m., May 9, 2012.
Place: The Westin Buckhead Atlanta, 3391 Peachtree Road, NE.,
Atlanta, Georgia, 30326, Telephone: (404) 365-0065.
Status: Open to the public, limited only by the space available.
The meeting room will accommodate approximately 100 people.
Purpose: This Committee is charged with advising the Director,
CDC and the Administrator, HRSA, regarding activities related to
prevention and control of HIV/AIDS and other STDs, the support of
health care services to persons living with HIV/AIDS, and education
of health professionals and the public about HIV/AIDS and other
STDs.
Matters To Be Discussed: Agenda items include: (1) Enhancing
Hepatitis Prevention Treatment and Care in the United States;
(2) Integrating HIV Prevention and Care Data Systems; (3)
External Peer Review of CDC Youth HIV/STI Prevention and Sexual
Health Activities; (4) Preparing for the Ryan White Reauthorization;
and (5) CHAC Workgroups Update.
Agenda items are subject to change as priorities dictate.
Contact Person for More Information: Margie Scott-Cseh, CDC,
National Center for HIV/AIDS, Viral Hepatitis, STD, and TB
Prevention, 1600 Clifton Road, NE., Mailstop E-07, Atlanta, Georgia
30333, Telephone (404) 639-8317.
The Director, Management Analysis and Services Office, has been
delegated the authority to sign Federal Register Notices pertaining
to announcements of meetings and other committee management
activities, for both the Centers for Disease Control and Prevention
and the Agency for Toxic Substances and Disease Registry.
Dated: April 16, 2012.
Elaine L. Baker,
Director, Management Analysis and Services Office, Centers for Disease
Control and Prevention.
[FR Doc. 2012-9549 Filed 4-19-12; 8:45 am]
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