Clinical Laboratory Improvement Advisory Committee, Centers for Disease Control and Prevention: Notice of Charter Renewal, 14805-14806 [2012-6080]
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Federal Register / Vol. 77, No. 49 / Tuesday, March 13, 2012 / Notices
The
Advisory Council on Alzheimer’s
Research, Care, and Services meets
quarterly to discuss programs that
impact people with Alzheimer’s disease
and related dementias and their
caregivers. The Advisory Council makes
recommendations about ways to reduce
the financial impact of Alzheimer’s
disease and related dementias and to
improve the health outcomes of people
with these conditions. The Advisory
Council provides feedback on the
National Plan to Address Alzheimer’s
Disease. On an annual basis, the
Advisory Council shall evaluate the
implementation of the
recommendations through an updated
national plan.
The Advisory Council consists of
designees from Federal agencies
including the Centers for Disease
Control and Prevention, Administration
on Aging, Centers for Medicare and
Medicaid Services, Indian Health
Service, Office of the Director of the
National Institutes of Health, National
Science Foundation, Department of
Veterans Affairs, Food and Drug
Administration, Agency for Healthcare
Research and Quality, and the Surgeon
General. The Advisory Council also
consists of 12 non-federal members
selected by the Secretary who are
Alzheimer’s patient advocates (2),
Alzheimer’s caregivers (2), health care
providers (2), representatives of State
health departments (2), researchers with
Alzheimer’s-related expertise in basic,
translational, clinical, or drug
development science (2), and voluntary
health association representatives (2).
Members serve for overlapping 4 year
terms, except that any member
appointed to fill a vacancy for an
unexpired term shall be appointed for
the remainder of such term. A member
may serve after the expiration of the
member’s term until a successor has
taken office. Members serve as Special
Government Employees. This
announcement is seeking nominations
for a ‘‘representative of a state public
health department’’ who is not a Federal
employee.
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SUPPLEMENTARY INFORMATION:
Sherry Glied,
Assistant Secretary for Planning and
Evaluation.
[FR Doc. 2012–6083 Filed 3–12–12; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention (CDC)
Request for Nominations of
Candidates to Serve on the Advisory
Committee on Immunization Practices
(ACIP)
The CDC is soliciting nominations for
membership on the ACIP. The ACIP
consists of 15 experts in fields
associated with immunization, who are
selected by the Secretary of the U. S.
Department of Health and Human
Services to provide advice and guidance
to the Secretary, the Assistant Secretary
for Health, and the CDC on the control
of vaccine-preventable diseases. The
role of the ACIP is to provide advice
that will lead to a reduction in the
incidence of vaccine preventable
diseases in the United States, and an
increase in the safe use of vaccines and
related biological products. The
committee also establishes, reviews, and
as appropriate, revises the list of
vaccines for administration to children
eligible to receive vaccines through the
Vaccines for Children (VFC) Program.
Nominations are being sought for
individuals who have expertise and
qualifications necessary to contribute to
the accomplishments of the committee’s
objectives. Nominees will be selected
based on expertise in the field of
immunization practices; multidisciplinary expertise in public health;
expertise in the use of vaccines and
immunologic agents in both clinical and
preventive medicine; knowledge of
vaccine development, evaluation, and
vaccine delivery; or knowledge about
consumer perspectives and/or social
and community aspects of
immunization programs. Federal
employees will not be considered for
membership. Members may be invited
to serve for four-year terms. The next
cycle of selection of candidates will
begin in the fall of 2012, for selection of
potential nominees to replace members
whose terms will end on June 30, 2013.
Selection of members is based on
candidates’ qualifications to contribute
to the accomplishment of ACIP
objectives (https://www.cdc.gov/
vaccines/recs/acip). The U.S.
Department of Health and Human
Services policy stipulates that
committee membership be balanced in
terms of points of view represented and
the committee’s function. Consideration
is given to a broad representation of
geographic areas within the U.S., as well
as gender, race, ethnicity, and persons
with disabilities. Nominees must be
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14805
U.S. citizens, and cannot be full-time
employees of the U.S. Government.
Candidates should submit the
following items:
• Current curriculum vitae, including
complete contact information
(telephone numbers, fax number,
mailing address, email address)
• At least one letter of
recommendation from person(s) not
employed by the U.S. Department of
Health and Human Services. Candidates
may submit letter(s) from current HHS
employees if they wish, but at least one
letter must be submitted by a person not
employed by HHS.
Nominations should be submitted
(postmarked or received) by November
16, 2012 (for consideration for term
beginning July 2013.) All files must be
submitted electronically as email
attachments to:
• Ms. Stephanie Thomas, c/o ACIP
Secretariat, SThomas5@cdc.gov.
• Nominations may be submitted by
the candidate or by the person/
organization recommending the
candidate.
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: March 6, 2012.
Elaine L. Baker,
Director, Management Analysis and Services
Office, Centers for Disease Control and
Prevention.
[FR Doc. 2012–6071 Filed 3–12–12; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
Clinical Laboratory Improvement
Advisory Committee, Centers for
Disease Control and Prevention:
Notice of Charter Renewal
This gives notice under the Federal
Advisory Committee Act (Pub. L. 92–
463) of October 6, 1972, that the Clinical
Laboratory Improvement Advisory
Committee, Centers for Disease Control
and Prevention (CDC), Department of
Health and Human Services (HHS), has
been renewed for a 2-year period
through February 19, 2014.
For information, contact May Chu,
Ph.D., Designated Federal Officer,
Clinical Laboratory Improvement
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14806
Federal Register / Vol. 77, No. 49 / Tuesday, March 13, 2012 / Notices
Advisory Committee, 1600 Clifton Road
NE., Mailstop E–94, Atlanta, Georgia
30333, telephone 404/498–6400 or fax
404/498–6410.
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: March 6, 2012.
Elaine L. Baker,
Director, Management Analysis and Services
Office, Centers for Disease Control and
Prevention.
[FR Doc. 2012–6080 Filed 3–12–12; 8:45 am]
BILLING CODE 4163–18–P
Dated: March 6, 2012.
Elaine L. Baker,
Director, Management Analysis and Services
Office, Centers for Disease Control and
Prevention.
[FR Doc. 2012–6075 Filed 3–12–12; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[Document Identifier: CMS–1880 and –1882;
CMS–10393; and CMS–R–245]
Agency Information Collection
Activities: Submission for OMB
Review; 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), Department of Health
and Human Services, is publishing the
following summary of proposed
collections 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 function;
(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: Extension without change of a
currently approved collection. Title of
Information Collection: Certification as
a Supplier of Portable X-Ray and
Portable X-Ray Survey Report Form and
Supporting Regulations at 42 CFR Part
486.100–486.110. Use: CMS–1880 is
initially completed by suppliers of
portable X-ray services, expressing an
interest in and requesting participation
in the Medicare program. This form
initiates the process of obtaining a
decision as to whether the conditions of
coverage are met as a portable X-ray
supplier. It also promotes data reduction
or introduction to, and retrieval from,
the Certification and Survey Provider
Enhanced Reporting (CASPER) by the
CMS Regional Offices (ROs).
CMS–1882 is used by the State survey
agency to provide data collected during
AGENCY:
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
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Disease, Disability, and Injury
Prevention and Control Special
Emphasis Panel (SEP): Initial Review
The meeting announced below
concerns Epidemiology, Prevention and
Treatment of Influenza and Other
Respiratory Infections in Ghana, Studies
at the Animal-Human Interface of
Influenza and Other Zoonotic Diseases
in Vietnam, The Incidence of
Community Associated Influenza and
Other Respiratory Infections in the
United States, and Epidemiology,
Prevention and Treatment of Influenza
and Other Respiratory Infections in
Panama and Central America Region,
Funding Opportunity Announcements
(FOAs) IP12–001, IP12–002,IP12–003,
and IP12–006, initial review.
Correction: The notice was published
in the Federal Register on January 26,
2012, Volume 77, Number 17, Page
4047. The place should read as follows:
Place: Crowne Plaza Hotel AtlantaAirport, 1325 Virginia Avenue, Atlanta,
GA 30344, Telephone: (404) 768–6660.
Contact Person for More Information:
Gregory Anderson, MPH, MS, Scientific
Review Officer, CDC, 1600 Clifton Road,
NE., Mailstop E60, Atlanta, Georgia
30333, Telephone: (404) 718–8833.
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.
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18:29 Mar 12, 2012
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an on-site survey of a supplier of
portable X-ray services to determine
compliance with the applicable
conditions of participation and to report
this information to the Federal
Government. The form is primarily a
coding worksheet designed to facilitate
data reduction and retrieval into the
ASPEN system at the CMS ROs. The
form includes basic information on
compliance (i.e., met, not met,
explanatory statements) and does not
require any descriptive information
regarding the survey activity itself. CMS
has the responsibility and authority for
certification decisions which are based
on supplier compliance with the
applicable conditions of participation.
The information needed to make these
decisions is available to CMS only
through the use of information
abstracted from the survey report form.
Subsequent to the publication of the
60-day Federal Register notice
(December 23, 2011; 76 FR 80372), the
Supporting Statement has been revised
by making editorial changes and by
adding clarifying language. The
requirements and burden estimates have
not changed. Form Numbers: CMS–1880
(Request for Certification as a Supplier
of Portable X-Ray Services), CMS–1882
(Medicare/Medicaid Portable X-Ray
Survey Report), and OCN 0938–0027.
Frequency: Occasionally. Affected
Public: State, Local, or Tribal
Governments. Number of Respondents:
579. Total Annual Responses: 86. Total
Annual Hours: 151. (For policy
questions regarding this collection
contact Georgia Johnson at 410–786–
6859. For all other issues call 410–786–
1326.)
2. Type of Information Collection
Request: Existing collection in use
without an OMB control number; Title
of Information Collection: Medicare
Beneficiary and Family-Centered
Satisfaction Survey; Use: The data
collection methodology used to
determine Beneficiary Satisfaction flows
from the proposed sampling approach.
While it was feasible to conduct the 9th
SOW via telephone data collection only,
with a quarterly sample size for the 10th
SOW estimated to be 2,664, it does not
seem efficient to maintain a telephone
only data collection approach. Based on
recent literature on survey methodology
and response rates by mode, we
recommend using a data collection that
is done primarily by mail. A mail-based
methodology will achieve the goals of
being efficient, effective, and minimally
burdensome for beneficiary
respondents.
As previously described, we
anticipate that a mail-based
methodology could yield a response rate
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[Federal Register Volume 77, Number 49 (Tuesday, March 13, 2012)]
[Notices]
[Pages 14805-14806]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2012-6080]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
Clinical Laboratory Improvement Advisory Committee, Centers for
Disease Control and Prevention: Notice of Charter Renewal
This gives notice under the Federal Advisory Committee Act (Pub. L.
92-463) of October 6, 1972, that the Clinical Laboratory Improvement
Advisory Committee, Centers for Disease Control and Prevention (CDC),
Department of Health and Human Services (HHS), has been renewed for a
2-year period through February 19, 2014.
For information, contact May Chu, Ph.D., Designated Federal
Officer, Clinical Laboratory Improvement
[[Page 14806]]
Advisory Committee, 1600 Clifton Road NE., Mailstop E-94, Atlanta,
Georgia 30333, telephone 404/498-6400 or fax 404/498-6410.
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: March 6, 2012.
Elaine L. Baker,
Director, Management Analysis and Services Office, Centers for Disease
Control and Prevention.
[FR Doc. 2012-6080 Filed 3-12-12; 8:45 am]
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