Agency Information Collection Activities: Proposed Collection; Comment Request, 1167-1168 [2011-140]
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Federal Register / Vol. 76, No. 5 / Friday, January 7, 2011 / Notices
Humphrey Building, 200 Independence
Avenue, SW., Washington, DC 20201.
Please allow sufficient time for mailed
comments to be received before the
close of the comment period. (Because
access to the interior of the Hubert H.
Humphrey Building is not readily
available to persons without Federal
government identification, commenters
are encouraged to leave their comments
in the OCIIO drop slots located in the
main lobby of the building. A stamp-in
clock is available for persons wishing to
retain a proof of filing by stamping in
and retaining an extra copy of the
comments being filed.)
3. By facsimile or E-mail to OMB.
OMB, Office of Information and
Regulatory Affairs, Attention: CMS Desk
Officer, Fax Number (202) 395–6974, Email: OIRA_submission@omb.eop.gov.
Dated: January 4, 2011.
Kenneth Cohen,
Director, Executive Secretariat & Regulatory
Affairs, Office of Consumer Information and
Insurance Oversight.
[FR Doc. 2011–142 Filed 1–6–11; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Meeting of the Presidential Advisory
Council on HIV/AIDS
Department of Health and
Human Services, Office of the Secretary,
Office of the Assistant Secretary for
Health.
ACTION: Notice.
AGENCY:
As stipulated by the Federal
Advisory Committee Act, the U.S.
Department of Health and Human
Service (DHHS) is hereby giving notice
that the Presidential Advisory Council
on HIV/AIDS (PACHA) will hold a
meeting. The meeting will be open to
the public.
DATES: The meeting will be held
Thursday, January 27, 2011 and Friday,
January 28, 2011. The meeting will be
held from 10 a.m. to approximately 5
p.m. on January 27, 2011 and 9 a.m. to
approximately 3 p.m. on January 28,
2011.
SUMMARY:
Department of Health and
Human Services, Room 800, Hubert H.
Humphrey Building, 200 Independence
Avenue, SW., Washington, DC 20201.
FOR FURTHER INFORMATION CONTACT: Mr.
Melvin Joppy, Committee Manager,
Presidential Advisory Council on HIV/
AIDS, Department of Health and Human
Services, 200 Independence Avenue,
Room 443H, Hubert H. Humphrey
Building, Washington, DC 20201; (202)
jdjones on DSK8KYBLC1PROD with NOTICES
ADDRESSES:
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1167
690–5560. More detailed information
about PACHA can be obtained by
accessing the Council’s Web site at
https://www.pacha.gov.
Dated: December 28, 2010.
Christopher H. Bates,
Executive Director, Presidential Advisory on
HIV/AIDS.
PACHA
was established by Executive Order
12963, dated June 14, 1995 as amended
by Executive Order 13009, dated June
14, 1996. The Council provides advice,
information, and recommendations to
the Secretary regarding programs and
policies to promote effective prevention
and cure of HIV disease and AIDS. The
functions of the Council are solely
advisory in nature.
The Council consists of not more than
25 members. Council members are
selected from prominent community
leaders with particular expertise in, or
knowledge of, matters concerning HIV
and AIDS, public health, global health,
philanthropy, marketing or business, as
well as other national leaders held in
high esteem from other sectors of
society. Council members are appointed
by the Secretary or designee, in
consultation with the White House
Office on National AIDS Policy. The
agenda and draft resolutions for the
upcoming meeting will be posted on the
Council’s Web site https://
www.pacha.gov.
Public attendance at the meeting is
limited to space available. Individuals
must provide a photo ID for entry into
the building. Individuals who plan to
attend and need special assistance, such
as language interpretation or reasonable
accommodations, should notify the
designated contact person. Preregistration for public attendance is
advisable and can be accomplished by
contacting the PACHA Committee
Manager.
Members of the public will have the
opportunity to provide comments on
January 28, 2011. Pre-registration is
required for public comment. Any
individual who wishes to participate in
the public comment session must
contact: Melvin Joppy, Office of HIV/
AIDS Policy, melvin.joppy@hhs.gov, by
close of business Monday, January 24,
2011. Public comment will be limited to
three minutes per speaker. Members of
the public who wish to have printed
materials distributed to PACHA
members for discussion at the meeting
are asked to provide, at a minimum, 30
copies of the materials to the PACHA
Committee Manager no later than close
of business Monday, January 24, 2011.
Contact information for the PACHA
Committee Manager is provided above.
[FR Doc. 2011–119 Filed 1–6–11; 8:45 am]
SUPPLEMENTARY INFORMATION:
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
Statement of Organization, Functions,
and Delegations of Authority
Part C (Centers for Disease Control
and Prevention) of the Statement of
Organization, Functions, and
Delegations of Authority of the
Department of Health and Human
Services (45 FR 67772–76, dated
October 14, 1980, and corrected at 45 FR
69296, October 20, 1980, as amended
most recently at 75 FR 70276–70277,
dated November 17, 2010) is amended
to reflect the title change for the Office
of Science Quality and Translation,
Office of the Associate Director for
Science, Office of the Director, Centers
for Disease Control and Prevention.
Section C–B, Organization and
Functions, is hereby amended as
follows:
Delete in its entirety the title for the
Office of Science Quality and
Translation (CASH) and insert the
Office of Science Quality (CASH).
Dated: December 29, 2010.
Barbara Harris,
Acting Chief Operating Officer, Centers for
Disease Control and Prevention (CDC).
[FR Doc. 2011–55 Filed 1–6–11; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[Document Identifier: CMS–10339]
Agency Information Collection
Activities: Proposed Collection;
Comment Request
Centers for Medicare &
Medicaid Services, HHS.
In compliance with the requirement
of section 3506(c)(2)(A) of the
Paperwork Reduction Act of 1995, the
Centers for Medicare & Medicaid
Services (CMS) is publishing the
following summary of proposed
collections for public comment.
Interested persons are invited to send
comments regarding this burden
AGENCY:
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Federal Register / Vol. 76, No. 5 / Friday, January 7, 2011 / Notices
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.
1. Type of Information Collection
Request: Revision of a currently
approved collection; Title of
Information Collection: Pre-Existing
Health Insurance Plan and Supporting
Regulations; Use: On March 23, 2010,
the President signed into law H.R. 3590,
the Patient Protection and Affordable
Care Act (Affordable Care Act), Public
Law 111–148. Section 1101 of the law
establishes a ‘‘temporary high risk health
insurance pool program’’ (which has
been named the Pre-Existing Condition
Insurance Plan, or PCIP) to provide
health insurance coverage to currently
uninsured individuals with pre-existing
conditions. The law authorizes HHS to
carry out the program directly or
through contracts with states or private,
non-profit entities.
We are requesting an extension of this
package because this information is
needed to assure that PCIP programs are
established timely and effectively. This
request is being made based on
regulations and guidance that have been
issued and contracts which have been
executed by HHS with States or an
entity on their behalf participating in
the PCIP program. PCIP is also referred
to as the temporary qualified high risk
insurance pool program, as it is called
in the Affordable Care Act, but we have
adopted the term PCIP to better describe
the program and avoid confusion with
the existing state high risk pool
programs. Form Number: CMS–10339
(OMB#: 0938–1100); Frequency:
Reporting—On occasion; Affected
Public: State governments; Number of
Respondents: 51; Total Annual
Responses: 2,652; Total Annual Hours:
36,924. (For policy questions regarding
this collection contact Laura Dash at
410–786–8623. For all other issues call
410–786–1326.)
To obtain copies of the supporting
statement and any related forms for the
proposed paperwork collections
referenced above, access CMS’ Web Site
at https://www.cms.hhs.gov/
PaperworkReductionActof1995, or Email your request, including your
address, phone number, OMB number,
and CMS document identifier, to
VerDate Mar<15>2010
15:30 Jan 06, 2011
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Paperwork@cms.hhs.gov, or call the
Reports Clearance Office on (410) 786–
1326.
In commenting on the proposed
information collections please reference
the document identifier or OMB control
number. To be assured consideration,
comments and recommendations must
be submitted in one of the following
ways by: March 8, 2011.
1. Electronically. You may submit
your comments electronically to https://
www.regulations.gov. Follow the
instructions for ‘‘Comment or
Submission’’ or ‘‘More Search Options’’
to find the information collection
document(s) accepting comments.
2. By regular mail. You may mail
written comments to the following
address: CMS, Office of Strategic
Operations and Regulatory Affairs,
Division of Regulations Development,
Attention: Document Identifier/OMB
Control Number, Room C4–26–05, 7500
Security Boulevard, Baltimore,
Maryland 21244–1850.
Dated: January 4, 2011.
Kenneth Cohen,
Director, Executive Secretariat & Regulatory
Affairs, Office of Consumer Information and
Insurance Oversight.
[FR Doc. 2011–140 Filed 1–6–11; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2011–N–0001]
Agency Information Collection
Activities; Proposed Collection;
Comment Request; Health and Diet
Survey
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice.
The Food and Drug
Administration (FDA) is announcing an
opportunity for public comment on the
proposed collection of certain
information by the Agency. Under the
Paperwork Reduction Act of 1995 (the
PRA), Federal Agencies are required to
publish notice in the Federal Register
concerning each proposed collection of
information, including each proposed
extension of an existing collection of
information, and to allow 60 days for
public comment in response to the
notice. This notice solicits comments on
FDA’s Health and Diet Survey.
DATES: Submit either electronic or
written comments on the collection of
information by March 8, 2011.
SUMMARY:
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Submit electronic
comments on the collection of
information to https://
www.regulations.gov. Submit written
comments on the collection of
information to the Division of Dockets
Management (HFA–305), Food and Drug
Administration, 5630 Fishers Lane, rm.
1061, Rockville, MD 20852. All
comments should be identified with the
docket number found in brackets in the
heading of this document.
FOR FURTHER INFORMATION CONTACT:
Denver Presley, Jr., Office of Information
Management, Food and Drug
Administration, 1350 Piccard Dr., PI50–
400B, Rockville, MD 20850, 301–796–
3793.
SUPPLEMENTARY INFORMATION: Under the
PRA (44 U.S.C. 3501–3520), Federal
Agencies must obtain approval from the
Office of Management and Budget
(OMB) for each collection of
information they conduct or sponsor.
‘‘Collection of information’’ is defined in
44 U.S.C. 3502(3) and 5 CFR 1320.3(c)
and includes Agency requests or
requirements that members of the public
submit reports, keep records, or provide
information to a third party. Section
3506(c)(2)(A) of the PRA (44 U.S.C.
3506(c)(2)(A)) requires Federal Agencies
to provide a 60-day notice in the
Federal Register concerning each
proposed collection of information,
including each proposed extension of an
existing collection of information,
before submitting the collection to OMB
for approval. To comply with this
requirement, FDA is publishing notice
of the proposed collection of
information set forth in this document.
With respect to the following
collection of information, FDA invites
comments on these topics: (1) Whether
the proposed collection of information
is necessary for the proper performance
of FDA’s functions, including whether
the information will have practical
utility; (2) the accuracy of FDA’s
estimate of the burden of the proposed
collection of information, including the
validity of the methodology and
assumptions used; (3) ways to enhance
the quality, utility, and clarity of the
information to be collected; and (4)
ways to minimize the burden of the
collection of information on
respondents, including through the use
of automated collection techniques,
when appropriate, and other forms of
information technology.
ADDRESSES:
Health and Diet Survey (OMB Control
Number 0910–0545—Extension)
FDA is seeking extension of OMB
approval for the Health and Diet Survey,
which is a voluntary consumer survey
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Agencies
[Federal Register Volume 76, Number 5 (Friday, January 7, 2011)]
[Notices]
[Pages 1167-1168]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2011-140]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Medicare & Medicaid Services
[Document Identifier: CMS-10339]
Agency Information Collection Activities: Proposed Collection;
Comment Request
AGENCY: Centers for Medicare & Medicaid Services, HHS.
In compliance with the requirement of section 3506(c)(2)(A) of the
Paperwork Reduction Act of 1995, the Centers for Medicare & Medicaid
Services (CMS) is publishing the following summary of proposed
collections for public comment. Interested persons are invited to send
comments regarding this burden
[[Page 1168]]
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.
1. Type of Information Collection Request: Revision of a currently
approved collection; Title of Information Collection: Pre-Existing
Health Insurance Plan and Supporting Regulations; Use: On March 23,
2010, the President signed into law H.R. 3590, the Patient Protection
and Affordable Care Act (Affordable Care Act), Public Law 111-148.
Section 1101 of the law establishes a ``temporary high risk health
insurance pool program'' (which has been named the Pre-Existing
Condition Insurance Plan, or PCIP) to provide health insurance coverage
to currently uninsured individuals with pre-existing conditions. The
law authorizes HHS to carry out the program directly or through
contracts with states or private, non-profit entities.
We are requesting an extension of this package because this
information is needed to assure that PCIP programs are established
timely and effectively. This request is being made based on regulations
and guidance that have been issued and contracts which have been
executed by HHS with States or an entity on their behalf participating
in the PCIP program. PCIP is also referred to as the temporary
qualified high risk insurance pool program, as it is called in the
Affordable Care Act, but we have adopted the term PCIP to better
describe the program and avoid confusion with the existing state high
risk pool programs. Form Number: CMS-10339 (OMB: 0938-1100);
Frequency: Reporting--On occasion; Affected Public: State governments;
Number of Respondents: 51; Total Annual Responses: 2,652; Total Annual
Hours: 36,924. (For policy questions regarding this collection contact
Laura Dash at 410-786-8623. For all other issues call 410-786-1326.)
To obtain copies of the supporting statement and any related forms
for the proposed paperwork collections referenced above, access CMS'
Web Site at https://www.cms.hhs.gov/PaperworkReductionActof1995, or E-
mail your request, including your address, phone number, OMB number,
and CMS document identifier, to Paperwork@cms.hhs.gov, or call the
Reports Clearance Office on (410) 786-1326.
In commenting on the proposed information collections please
reference the document identifier or OMB control number. To be assured
consideration, comments and recommendations must be submitted in one of
the following ways by: March 8, 2011.
1. Electronically. You may submit your comments electronically to
https://www.regulations.gov. Follow the instructions for ``Comment or
Submission'' or ``More Search Options'' to find the information
collection document(s) accepting comments.
2. By regular mail. You may mail written comments to the following
address: CMS, Office of Strategic Operations and Regulatory Affairs,
Division of Regulations Development, Attention: Document Identifier/OMB
Control Number, Room C4-26-05, 7500 Security Boulevard, Baltimore,
Maryland 21244-1850.
Dated: January 4, 2011.
Kenneth Cohen,
Director, Executive Secretariat & Regulatory Affairs, Office of
Consumer Information and Insurance Oversight.
[FR Doc. 2011-140 Filed 1-6-11; 8:45 am]
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