Agency Information Collection Request; 60-Day Public Comment Request, 4819-4820 [2012-2038]
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4819
Federal Register / Vol. 77, No. 20 / Tuesday, January 31, 2012 / Notices
recordkeeping requirements for
qualified financial contracts (QFCs) held
by insured depository institutions in
troubled condition.
Request for Comment
Comments are invited on: (a) Whether
the collection of information is
necessary for the proper performance of
the FDIC’s functions, including whether
the information has practical utility; (b)
the accuracy of the estimates of the
burden of the information collection,
including the validity of the
methodology and assumptions used; (c)
ways to enhance the quality, utility, and
clarity of the information to be
collected; and (d) ways to minimize the
burden of the information collection on
respondents, including through the use
of automated collection techniques or
other forms of information technology.
All comments will become a matter of
public record.
Dated at Washington, DC, this 25th day of
January, 2012.
Federal Deposit Insurance Corporation.
Robert E. Feldman,
Executive Secretary.
appointing authority relative to the
performance of the senior executive.
Richard A. Lidinsky, Jr.,
Chairman.
The Members of the Performance
Review Board:
1. Joseph E. Brennan, Commissioner
2. Mario Cordero, Commissioner
3. Rebecca F. Dye, Commissioner
4. Michael A. Khouri, Commissioner
5. Clay G. Guthridge, Administrative Law
Judge
6. Erin M. Wirth, Administrative Law Judge
7. Florence A. Carr, Deputy Managing
Director
8. Lowry A. Crook, Chief of Staff
9. Rebecca A. Fenneman, General Counsel
10. Karen V. Gregory, Secretary
11. Vern W. Hill, Director, Office of
Consumer Affairs and Dispute
Resolution Services
12. Peter J. King, Director, Bureau of
Enforcement
13. Sandra L. Kusumoto, Director, Bureau of
Certification and Licensing
14. Ronald D. Murphy, Managing Director
15. Austin L. Schmitt, Director, Bureau of
Trade Analysis
[FR Doc. 2012–1982 Filed 1–30–12; 8:45 am]
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[FR Doc. 2012–1949 Filed 1–30–12; 8:45 am]
BILLING CODE 6714–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
[Document Identifier OS–0990–0260]
FEDERAL MARITIME COMMISSION
Agency Information Collection
Request; 60-Day Public Comment
Request
Performance Review Board
Federal Maritime Commission.
Notice.
AGENCY:
ACTION:
Notice is hereby given of the
names of the members of the
Performance Review Board.
FOR FURTHER INFORMATION CONTACT:
Harriette H. Charbonneau, Director of
Human Resources, Federal Maritime
Commission, 800 North Capitol Street
NW., Washington, DC 20573.
SUPPLEMENTARY INFORMATION: Section
4314(c)(1) through (5) of title 5, U.S.C.,
requires each agency to establish, in
accordance with regulations prescribed
by the Office of Personnel Management,
one or more performance review boards.
The board shall review and evaluate the
initial appraisal of a senior executive’s
performance by the supervisor, along
with any recommendations to the
wreier-aviles on DSK5TPTVN1PROD with NOTICES
SUMMARY:
Office of the Secretary, HHS.
In compliance with the requirement
of section 3506(c)(2)(A) of the
Paperwork Reduction Act of 1995, the
Office of the Secretary (OS), Department
of Health and Human Services (HHS), is
publishing the following summary of a
proposed information collection request
for public comment. Interested persons
are invited to send comments regarding
this burden estimate or any other aspect
of this collection of information,
including any of the following subjects:
(1) The necessity and utility of the
proposed information collection for the
proper performance of the agency’s
functions; (2) the accuracy of the
estimated burden; (3) ways to enhance
the quality, utility, and clarity of the
information to be collected; and (4) the
use of automated collection techniques
AGENCY:
or other forms of information
technology to minimize the information
collection burden.
To obtain copies of the supporting
statement and any related forms for the
proposed paperwork collections
referenced above, email your request,
including your address, phone number,
OMB number, and OS document
identifier, to
Sherette.funncoleman@hhs.gov, or call
the Reports Clearance Office on (202)
690–5683. Written comments and
recommendations for the proposed
information collections must be directed
to the OS Paperwork Clearance Officer
at the above email address within 60
days.
Proposed Project: Protection of
Human Subjects: Assurance of
Compliance with Federal Policy/IRB
Review/IRB Recordkeeping/Informed
Consent/Consent Documentation—OMB
No. 0990–0260—Office for Human
Research Protections.
Abstract: Section 491(a) of Public Law
99–158 states that the Secretary of HHS
shall by regulation require that each
entity applying for HHS support (e.g., a
grant, contract, or cooperative
agreement) to conduct research
involving human subjects submit to
HHS assurances satisfactory to the
Secretary that it has established an
institutional review board (IRB) to
review the research in order to ensure
protection of the rights and welfare of
the human research subjects. IRBs are
boards, committees, or groups formally
designated by an entity to review,
approve, and have continuing oversight
of research involving human subjects.
Pursuant to the requirement of the
Public Law 99–158, HHS promulgated
regulations at 45 CFR part 46, subpart A,
the basic HHS Policy for the Protection
of Human Subjects. The June 18, 1991
adoption of the common Federal Policy
(56 FR 28003) by 15 departments and
agencies implements a recommendation
of the President’s Commission for the
Study of Ethical Problems in Medicine
and Biomedical and Behavioral
Research which was established on
November 9, 1974, by Public Law 95–
622. The Common Rule is based on HHS
regulations at 45 CFR part 46, subpart A,
the basic HHS Policy for the Protection
of Human Subjects.
TOTAL ESTIMATED ANNUALIZED BURDEN—DOLLARS
Total burden
hours
Total .............................................................................................................................................
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1,138,000
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31JAN1
Hourly wage
rate
$23.20
Total burden
dollars
$26,400,000
4820
Federal Register / Vol. 77, No. 20 / Tuesday, January 31, 2012 / Notices
Keith A. Tucker,
Paperwork Reduction Act Clearance Officer,
Office of the Secretary.
[FR Doc. 2012–2038 Filed 1–30–12; 8:45 am]
BILLING CODE 4150–36–P
Dated: January 25, 2012.
Elaine L. Baker,
Director, Management Analysis and Services
Office, Centers for Disease Control and
Prevention.
[FR Doc. 2012–2001 Filed 1–30–12; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
Healthcare Infection Control Practices
Advisory Committee (HICPAC)
Centers for Disease Control and
Prevention
wreier-aviles on DSK5TPTVN1PROD with NOTICES
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) announce
the following meeting for the
aforementioned committee:
World Trade Center Health Program
Scientific/Technical Advisory
Committee (WTCHP STAC or Advisory
Committee), National Institute for
Occupational Safety and Health
(NIOSH)
Times and Dates: 9 a.m.–5 p.m., February
16, 2012, 9 a.m.–12 p.m., February 17, 2012.
Place: CDC, Global Communications
Center, Building 19, Auditorium B3, 1600
Clifton Road NE., Atlanta, Georgia 30333.
Status: Open to the public, limited only by
the space available. Please register for the
meeting at www.cdc.gov/hicpac.
Purpose: The Committee is charged with
providing advice and guidance to the
Secretary, the Assistant Secretary for Health
and Human Services, the Director, CDC, the
Director, National Center for Emerging and
Zoonotic Infectious Diseases (NCEZID), and
the Director, Division of Healthcare Quality
Promotion regarding (1) the practice of
healthcare infection control; (2) strategies for
surveillance, prevention, and control of
infections (e.g., nosocomial infections),
antimicrobial resistance, and related events
in settings where healthcare is provided; and
(3) periodic updating of guidelines and other
policy statements regarding prevention of
healthcare-associated infections and
healthcare-related conditions.
Matters To Be Discussed: The agenda will
include updates on CDC’s activities for
Healthcare Associated Infections (HAI),
CDC’s dialysis HAI activities, and CDC’s
long-term care HAI activities, draft guideline
for prevention of infections among patients
in neonatal intensive care units (NICU), draft
guideline for infection control in healthcare
personnel, draft guideline for the prevention
of surgical site infections, update from the
HICPAC surveillance working group, and
updates on HAI surveillance definitions.
Agenda items are subject to change as
priorities dictate.
Contact Person for More Information: Erin
Stone, M.S., HICPAC, Division of Healthcare
Quality Promotion, NCEZID, CDC, l600
Clifton Road NE., Mailstop A–07, Atlanta,
Georgia 30333, Telephone: (404) 639–8692,
Email: hicpac@cdc.gov.
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.
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),
announces the following meetings of the
aforementioned committee:
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Committee Public Meeting Times and
Dates: (All times are Eastern Standard Time.)
12 p.m.–5 p.m., February 15, 2012. 8:30
a.m.–2 p.m., February 16, 2012.
Public Comment Times and Dates: (All
times are Eastern Standard Time.)
3:45 p.m.–4:45 p.m., on February 15, 2012.
8:45 a.m.–9:45 a.m., on February 16, 2012.
Place: Jacob J. Javits Federal Building, 26
Federal Plaza, New York, New York 10278.
This meeting is also available by
teleconference. Please dial 1–800–593–0693
and enter code 37121.
Status: Open to the public, limited by the
capacity of the room, which is about 70
persons, and the number of telephone lines.
The conference line will accommodate up to
300 callers; therefore it is suggested that
those interested in calling in to listen to the
committee meeting share a line when
possible.
Please note that the public comment
periods end at the times indicated above or
following the last call for comments,
whichever is earlier. Members of the public
who want to comment must sign up. A
limited number of time slots are available
and will be assigned on a first come-first
served basis. Each commenter will be
provided up to five minutes for comment.
You can sign up before the meeting by mail,
facsimile, email, or telephone until all slots
are filled. When you sign up you must
indicate if you will be making your
comments by telephone or in person.
Advance sign up will conclude at 5 p.m. on
February 13, 2012. If time slots are still
available, you will be able to sign up at the
meeting beginning at 11 a.m. on February 15
for the public comment period that day, or
beginning at 8 a.m. on February 16, for the
public comment period that day. To sign up
in advance of the meeting, use the contact
information that follows.
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Mail: NIOSH Docket Office, Robert A. Taft
Laboratories, MS–C–34, 4676 Columbia
Parkway, Cincinnati, Ohio 45226.
Facsimile: (513) 533–8285.
Email: nioshdocket@cdc.gov.
Telephone: (513) 533–8611.
Written comments will also be accepted
(see below).
Security Considerations: Due to mandatory
security clearance procedures at the Jacob K.
Javits Federal Building, in-person attendees
must present valid government-issued
picture identification to security personnel
upon entering the building and go through an
airport-type security check. Non-U.S. citizens
are encouraged to participate in the audio
conferencing due to the extra clearance
involved with in-person attendance. To
attend in person, a non-U.S. citizen will have
to call or send an email to the contact person
in this Notice before February 1, 2012, and
provide passport information. You will be
notified if clearance to attend the meeting in
person is received; otherwise, you will not be
able to attend the meeting in person.
Background: The Advisory Committee was
established by Public Law 111–347 (The
James Zadroga 9/11 Health and
Compensation Act of 2010, Title XXXIII of
the Public Health Service Act), enacted on
January 2, 2011 and codified at 42 U.S.C.
300mm–300mm–61.
Purpose: The purpose of the Advisory
Committee is to review scientific and
medical evidence and to make
recommendations to the World Trade Center
(WTC) Program Administrator regarding
additional WTC Health Program eligibility
criteria and potential additions to the list of
covered WTC-related health conditions. Title
XXXIII of the Public Health Service Act
established within the Department of Health
and Human Services (HHS), the World Trade
Center (WTC) Health Program, to be
administered by the WTC Program
Administrator. The WTC Health Program
provides: (1) Medical monitoring and
treatment benefits to eligible emergency
responders and recovery and cleanup
workers (including those who are Federal
employees) who responded to the September
11, 2001, terrorist attacks, and (2) initial
health evaluation, monitoring, and treatment
benefits to residents and other building
occupants and area workers in New York
City, who were directly impacted and
adversely affected by such attacks
(‘‘survivors’’). Certain specific activities of
the WTC Program Administrator are reserved
to the Secretary, HHS, to delegate at her
discretion; other WTC Program
Administrator duties not explicitly reserved
to the Secretary, HHS, are assigned to the
Director, NIOSH. The administration of the
Advisory Committee established under
Section 300mm–1(a) is left to the Director of
NIOSH in his role as WTC Program
Administrator. CDC and NIOSH provide
funding, staffing, and administrative support
services for the Advisory Committee. The
charter was issued on May 12, 2011, and will
expire on May 12, 2013.
Matters To Be Discussed: The agenda for
the Advisory Committee meeting includes:
discussion of the petition to add cancer to the
list of covered WTC-related health
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]]>Agencies
[Federal Register Volume 77, Number 20 (Tuesday, January 31, 2012)]
[Notices]
[Pages 4819-4820]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2012-2038]
=======================================================================
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
[Document Identifier OS-0990-0260]
Agency Information Collection Request; 60-Day Public Comment
Request
AGENCY: Office of the Secretary, HHS.
In compliance with the requirement of section 3506(c)(2)(A) of the
Paperwork Reduction Act of 1995, the Office of the Secretary (OS),
Department of Health and Human Services (HHS), is publishing the
following summary of a proposed information collection request for
public comment. Interested persons are invited to send comments
regarding this burden estimate or any other aspect of this collection
of information, including any of the following subjects: (1) The
necessity and utility of the proposed information collection for the
proper performance of the agency's functions; (2) the accuracy of the
estimated burden; (3) ways to enhance the quality, utility, and clarity
of the information to be collected; and (4) the use of automated
collection techniques or other forms of information technology to
minimize the information collection burden.
To obtain copies of the supporting statement and any related forms
for the proposed paperwork collections referenced above, email your
request, including your address, phone number, OMB number, and OS
document identifier, to Sherette.funncoleman@hhs.gov, or call the
Reports Clearance Office on (202) 690-5683. Written comments and
recommendations for the proposed information collections must be
directed to the OS Paperwork Clearance Officer at the above email
address within 60 days.
Proposed Project: Protection of Human Subjects: Assurance of
Compliance with Federal Policy/IRB Review/IRB Recordkeeping/Informed
Consent/Consent Documentation--OMB No. 0990-0260--Office for Human
Research Protections.
Abstract: Section 491(a) of Public Law 99-158 states that the
Secretary of HHS shall by regulation require that each entity applying
for HHS support (e.g., a grant, contract, or cooperative agreement) to
conduct research involving human subjects submit to HHS assurances
satisfactory to the Secretary that it has established an institutional
review board (IRB) to review the research in order to ensure protection
of the rights and welfare of the human research subjects. IRBs are
boards, committees, or groups formally designated by an entity to
review, approve, and have continuing oversight of research involving
human subjects.
Pursuant to the requirement of the Public Law 99-158, HHS
promulgated regulations at 45 CFR part 46, subpart A, the basic HHS
Policy for the Protection of Human Subjects. The June 18, 1991 adoption
of the common Federal Policy (56 FR 28003) by 15 departments and
agencies implements a recommendation of the President's Commission for
the Study of Ethical Problems in Medicine and Biomedical and Behavioral
Research which was established on November 9, 1974, by Public Law 95-
622. The Common Rule is based on HHS regulations at 45 CFR part 46,
subpart A, the basic HHS Policy for the Protection of Human Subjects.
Total Estimated Annualized Burden--Dollars
----------------------------------------------------------------------------------------------------------------
Total burden Hourly wage Total burden
hours rate dollars
----------------------------------------------------------------------------------------------------------------
Total........................................................... 1,138,000 $23.20 $26,400,000
----------------------------------------------------------------------------------------------------------------
[[Page 4820]]
Keith A. Tucker,
Paperwork Reduction Act Clearance Officer, Office of the Secretary.
[FR Doc. 2012-2038 Filed 1-30-12; 8:45 am]
BILLING CODE 4150-36-P
