Meeting of the National Biodefense Science Board, 52950-52951 [2010-21504]
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Federal Register / Vol. 75, No. 167 / Monday, August 30, 2010 / Notices
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20892. The meeting will be open to the
public with attendance limited to space
available. The meeting will also be Web
cast.
The main agenda item will be a
review of the revised draft report on
genetics education and training and
discussion of the final draft
recommendations. The meeting will
also include sessions on genomic data
sharing and the implications of
affordable whole-genome sequencing,
an update on the implementation of the
Genetic Information Nondiscrimination
Act, and a briefing from the Food and
Drug Administration on activities
related to genetic testing.
As always, the Committee welcomes
hearing from anyone wishing to provide
public comment on any issue related to
genetics, health and society. Please note
that because SACGHS operates under
the provisions of the Federal Advisory
Committee Act, all public comments
will be made available to the public.
Individuals who would like to provide
public comment should notify the
SACGHS Executive Secretary, Ms. Sarah
Carr, by telephone at 301–496–9838 or
e-mail at carrs@od.nih.gov. The
SACGHS office is located at 6705
Rockledge Drive, Suite 750, Bethesda,
MD 20892. Anyone planning to attend
the meeting who needs special
assistance, such as sign language
interpretation or other reasonable
accommodations, is also asked to
contact the Executive Secretary.
Under authority of 42 U.S.C. 217a,
Section 222 of the Public Health Service
Act, as amended, the Department of
Health and Human Services established
SACGHS to serve as a public forum for
deliberations on the broad range of
human health and societal issues raised
by the development and use of genetic
and genomic technologies and, as
warranted, to provide advice on these
issues. The draft meeting agenda and
other information about SACGHS,
including information about access to
the Web cast, will be available at the
following Web site: https://
oba.od.nih.gov/SACGHS/
sacghs_meetings.html.
Dated: August 24, 2010.
Jennifer Spaeth,
Director, NIH Office of Federal Advisory
Committee Policy.
[FR Doc. 2010–21532 Filed 8–27–10; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Committee on Vital and Health
Statistics: Meeting
Pursuant to the Federal Advisory
Committee Act, the Department of
Health and Human Services (HHS)
announces the following advisory
committee meeting.
Name: National Committee on Vital and
Health Statistics (NCVHS), Full Committee
Meeting.
Time and Date: September 15, 2010 9 a.m.–
2 p.m.; September 16, 2010 8:30 a.m.–
12:30 p.m.
Place: Embassy Suites Crystal City Hotel,
1300 Jefferson Davis Highway, Arlington, VA
22202, (703) 979–9799.
Status: Open.
Purpose: At this meeting the Committee
will hear presentations and hold discussions
on several health data policy topics. On the
morning of the first day the Committee will
hear updates from the Department, the Center
for Medicare and Medicaid Services, and the
Office of the National Coordinator for Health
Information Technology. Draft letters to the
HHS Secretary regarding the HIPAA national
health plan identifier and operating rules on
eligibility and claim status will also be
discussed. In the afternoon there will be a
discussion about a letter to the HHS
Secretary regarding sensitive information in
medical records.
On the morning of the second day there
will be a review of the final letters regarding
the national health plan identifier, operating
rules on eligibility and claim status, and
sensitive information in medical records.
Subcommittees will also present their
reports. The afternoon of the second day will
conclude with a discussion of the 60th
Anniversary Symposium that was held in
June 2010.
The times shown above are for the full
Committee meeting. Subcommittee breakout
sessions can be scheduled for late in the
afternoon of the first day and second day and
in the morning prior to the full Committee
meeting on the second day. Agendas for these
breakout sessions will be posted on the
NCVHS Web site (URL below) when
available.
Contact Person for More Information:
Substantive program information as well as
summaries of meetings and a roster of
committee members may be obtained from
Marjorie S. Greenberg, Executive Secretary,
NCVHS, National Center for Health Statistics,
Centers for Disease Control and Prevention,
3311 Toledo Road, Room 2402, Hyattsville,
Maryland 20782, telephone (301) 458–4245.
Information also is available on the NCVHS
home page of the HHS Web site: https://
www.ncvhs.hhs.gov/, where further
information including an agenda will be
posted when available.
Should you require reasonable
accommodation, please contact the CDC
Office of Equal Employment Opportunity on
(301) 458–4EEO (4336) as soon as possible.
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Dated: August 24, 2010.
James Scanlon,
Deputy Assistant Secretary for Planning and
Evaluation (Science and Data Policy), Office
of the Assistant Secretary for Planning and
Evaluation.
[FR Doc. 2010–21516 Filed 8–27–10; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Meeting of the National Biodefense
Science Board
Department of Health and
Human Services, Office of the Secretary.
ACTION: Notice.
AGENCY:
As stipulated by the Federal
Advisory Committee Act, the U.S.
Department of Health and Human
Services is hereby giving notice that the
National Biodefense Science Board
(NBSB) will be holding a public
meeting. The meeting is open to the
public.
SUMMARY:
The NBSB will hold a public
meeting on September 22, 2010 from 8
a.m. to 5 p.m. ET. The agenda is subject
to change as priorities dictate.
ADDRESSES: Washington, DC Metro
Area. The venue details will be posted
on the NBSB webpage at https://
www.phe.gov/Preparedness/legal/
boards/nbsb/Pages/default.aspx as they
become available.
FOR FURTHER INFORMATION CONTACT: Email: NBSB@HHS.GOV.
SUPPLEMENTARY INFORMATION: Pursuant
to section 319M of the Public Health
Service Act (42 U.S.C. 247d–7f) and
section 222 of the Public Health Service
Act (42 U.S.C. 217a), the Department of
Health and Human Services established
the National Biodefense Science Board.
The Board shall provide expert advice
and guidance to the Secretary on
scientific, technical, and other matters
of special interest to the Department of
Health and Human Services regarding
current and future chemical, biological,
nuclear, and radiological agents,
whether naturally occurring, accidental,
or deliberate. The Board may also
provide advice and guidance to the
Secretary on other matters related to
public health emergency preparedness
and response.
Background: A portion of this public
meeting will be dedicated to a report
and presentation by the Disaster Mental
Health Subcommittee to the NBSB on
their assessment of the Department of
Health and Human Services’ progress to
better integrate behavioral health into
emergency preparedness and response
DATES:
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52951
Federal Register / Vol. 75, No. 167 / Monday, August 30, 2010 / Notices
activities. Subsequent agenda topics
will be added as priorities dictate.
Availability of Materials: The meeting
agenda and materials will be posted on
the NBSB Web site at https://
www.phe.gov/Preparedness/legal/
boards/nbsb/Pages/default.aspx prior to
the meeting.
Procedures for Providing Public Input:
Any member of the public providing
oral comments at the meeting must sign
in at the registration desk and provide
his/her name, address, and affiliation.
All written comments must be received
prior to September 21, and should be
sent by e-mail to NBSB@HHS.GOV with
‘‘NBSB Public Comment’’ as the subject
line. Individuals who plan to attend and
need special assistance, such as sign
language interpretation or other
reasonable accommodations, should
e-mail NBSB@HHS.GOV.
Dated: August 10, 2010.
Nicole Lurie,
Assistant Secretary for Preparedness and
Response.
[FR Doc. 2010–21504 Filed 8–27–10; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Agency for Healthcare Research and
Quality
Agency Information Collection
Activities: Proposed Collection;
Comment Request
Agency for Healthcare Research
and Quality, HHS.
ACTION: Notice.
AGENCY:
This notice announces the
intention of the Agency for Healthcare
Research and Quality (AHRQ) to request
that the Office of Management and
Budget (OMB) approve the proposed
information collection project:
‘‘Understanding Patients’ Knowledge
and Use of Acetaminophen—Phase 2.’’
In accordance with the Paperwork
Reduction Act, 44 U.S.C. 3501–3520,
AHRQ invites the public to comment on
this proposed information collection.
DATES: Comments on this notice must be
received by October 29, 2010.
SUMMARY:
Written comments should
be submitted to: Doris Lefkowitz,
Reports Clearance Officer, AHRQ, by email at doris.lefkowitz@AHRQ.hhs.gov.
Copies of the proposed collection plans,
data collection instruments, and specific
details on the estimated burden can be
obtained from the AHRQ Reports
Clearance Officer.
FOR FURTHER INFORMATION CONTACT:
Doris Lefkowitz, AHRQ Reports
Clearance Officer, (301) 427–1477, or by
e-mail at
doris.lefkowitz@AHRQ.hhs.gov.
ADDRESSES:
SUPPLEMENTARY INFORMATION:
Proposed Project
Understanding Patients’ Knowledge and
Use of Acetaminophen—Phase 2
AHRQ proposes a cross-sectional
prospective survey to identify issues
that relate to the misuse and overdosing
of over-the-counter (OTC)
acetaminophen. The survey was
developed based on results from a
previous data collection (OMB control
number 0935–0154, approved on 10/13/
2009). Acetaminophen is the most
widely used analgesic and antipyretic
drug in the U.S. When appropriately
used, it is a very safe agent. However,
a single large overdose, or several
supratherapeutic dosages in a short
period of time, has been associated with
acute liver failure, which can occur with
dosages over 250 mg/kg over a 24-hour
period, or > 12 g in an adult. Toxicity
from acetaminophen has been on the
rise in the past 3 decades, and is now
the most common cause of acute liver
failure in the U.S., surpassing viral
hepatitis.
This project has the following aims:
(1) To estimate frequency of use,
knowledge, and practices regarding use
of OTC acetaminophen, and
(2) To evaluate potential determinants
of misuse in community-based samples.
This information will be useful for
policy makers to consider and to
evaluate regulations and legislation with
respect to the distribution, dispensing
and sales of OTC acetaminophen.
This study is being conducted by
AHRQ through its contractor, the
University of Texas. This project
supports AHRQ’s Centers for Education
and Research on Therapeutics initiative
to promote the safe and effective use of
therapeutics. See 42 U.S.C. 299b–1(b). It
also supports AHRQ’s mandate for the
inclusion of priority populations. See 42
U.S.C. 299(c).
Method of Collection
To achieve the projects’ aims the
following data collections will be
implemented:
(1) Surveys with parents of young
children (age < 8 years). The purpose of
this survey is to learn how parents
administer acetaminophen to their
children and to identify determinants of
misuse of acetaminophen;
(2) Surveys with adolescents (ages 13
to 20). The purpose of this survey is to
learn how adolescents use
acetaminophen and to identify
determinants of misuse of
acetaminophen;
(3) Surveys with adults (21 to 65 years
of age). The purpose of this survey is to
learn how adults use acetaminophen
and to identify determinants of misuse
of acetaminophen;
(4) Surveys with adults (greater than
65 years of age). The purpose of this
survey is to learn how older adults use
acetaminophen and to identify
determinants of misuse of
acetaminophen, particularly in regards
to age-related factors.
Data will be collected in person using
paper questionnaires administered by
the project personnel.
Estimated Annual Respondent Burden
Exhibit 1 shows the estimated
annualized burden hours for the
respondent’s time to participate in this
project. Each of the four questionnaires
used in the planned face-to-face surveys
will require approximately 30 minutes
to complete. The total annualized
burden for all participants is estimated
to be 400 hours.
Exhibit 2 shows the estimated
annualized cost burden for the
respondent’s time to participate in the
project. The total annualized cost
burden is estimated to be $8,361.
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EXHIBIT 1—ESTIMATED ANNUALIZED BURDEN HOURS
Number of
respondents
Data collection mode
Surveys
Surveys
Surveys
Surveys
with
with
with
with
VerDate Mar<15>2010
Parents of Children < 8 years of age .........................................
Adolescents (13 to 20 years of age) .........................................
Adults (20 to 65 years) ..............................................................
Adults (greater than 65 years) ...................................................
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Number of
responses per
respondent
300
200
150
150
E:\FR\FM\30AUN1.SGM
1
1
1
1
30AUN1
Hours
per response
30/60
30/60
30/60
30/60
Total
burden
hours
150
100
75
75
Agencies
[Federal Register Volume 75, Number 167 (Monday, August 30, 2010)]
[Notices]
[Pages 52950-52951]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2010-21504]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Meeting of the National Biodefense Science Board
AGENCY: Department of Health and Human Services, Office of the
Secretary.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: As stipulated by the Federal Advisory Committee Act, the U.S.
Department of Health and Human Services is hereby giving notice that
the National Biodefense Science Board (NBSB) will be holding a public
meeting. The meeting is open to the public.
DATES: The NBSB will hold a public meeting on September 22, 2010 from 8
a.m. to 5 p.m. ET. The agenda is subject to change as priorities
dictate.
ADDRESSES: Washington, DC Metro Area. The venue details will be posted
on the NBSB webpage at https://www.phe.gov/Preparedness/legal/boards/nbsb/Pages/default.aspx as they become available.
FOR FURTHER INFORMATION CONTACT: E-mail: NBSB@HHS.GOV.
SUPPLEMENTARY INFORMATION: Pursuant to section 319M of the Public
Health Service Act (42 U.S.C. 247d-7f) and section 222 of the Public
Health Service Act (42 U.S.C. 217a), the Department of Health and Human
Services established the National Biodefense Science Board. The Board
shall provide expert advice and guidance to the Secretary on
scientific, technical, and other matters of special interest to the
Department of Health and Human Services regarding current and future
chemical, biological, nuclear, and radiological agents, whether
naturally occurring, accidental, or deliberate. The Board may also
provide advice and guidance to the Secretary on other matters related
to public health emergency preparedness and response.
Background: A portion of this public meeting will be dedicated to a
report and presentation by the Disaster Mental Health Subcommittee to
the NBSB on their assessment of the Department of Health and Human
Services' progress to better integrate behavioral health into emergency
preparedness and response
[[Page 52951]]
activities. Subsequent agenda topics will be added as priorities
dictate.
Availability of Materials: The meeting agenda and materials will be
posted on the NBSB Web site at https://www.phe.gov/Preparedness/legal/boards/nbsb/Pages/default.aspx prior to the meeting.
Procedures for Providing Public Input: Any member of the public
providing oral comments at the meeting must sign in at the registration
desk and provide his/her name, address, and affiliation. All written
comments must be received prior to September 21, and should be sent by
e-mail to NBSB@HHS.GOV with ``NBSB Public Comment'' as the subject
line. Individuals who plan to attend and need special assistance, such
as sign language interpretation or other reasonable accommodations,
should e-mail NBSB@HHS.GOV.
Dated: August 10, 2010.
Nicole Lurie,
Assistant Secretary for Preparedness and Response.
[FR Doc. 2010-21504 Filed 8-27-10; 8:45 am]
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