Agency Recordkeeping/Reporting Requirements Under Emergency Review by the Office of Management and Budget (OMB), 38183-38184 [2011-16290]
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Federal Register / Vol. 76, No. 125 / Wednesday, June 29, 2011 / Notices
under review (sets 7–10); OCAS dose
reconstruction quality management and
assurance activities.
The agenda is subject to change as
priorities dictate.
In the event an individual cannot attend,
written comments may be submitted. Any
written comments received will be provided
at the meeting and should be submitted to
the contact person below well in advance of
the meeting.
Contact Person for more Information:
Theodore Katz, Executive Secretary, NIOSH,
CDC, 1600 Clifton Road, Mailstop E–20,
Atlanta, Georgia 30333, Telephone (513)
533–6800, Toll Free 1(800) CDC–INFO, email ocas@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.
Dated: June 23, 2011.
Elaine L. Baker,
Director, Management Analysis and Services
Office, Centers for Disease Control and
Prevention.
[FR Doc. 2011–16402 Filed 6–28–11; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
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Subcommittee on Procedures Review,
Advisory Board on Radiation and
Worker Health (ABRWH), National
Institute for Occupational Safety and
Health (NIOSH)
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 meeting for the
aforementioned subcommittee:
TIME AND DATE: 9 a.m.–5 p.m., July 14,
2011.
PLACE: Cincinnati Airport Marriott,
2395 Progress Drive, Hebron, Kentucky
41018, Telephone (859)334–4611, Fax
(859)334–4619.
STATUS: Open to the public, but without
a public comment period. To access by
conference call dial the following
information: (866)659–0537, Participant
Pass Code 9933701.
Background: The ABRWH was
established under the Energy Employees
Occupational Illness Compensation
Program Act of 2000 to advise the
President on a variety of policy and
technical functions required to
implement and effectively manage the
compensation program. Key functions of
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the ABRWH include providing advice
on the development of probability of
causation guidelines that have been
promulgated by the Department of
Health and Human Services (HHS) as a
final rule; advice on methods of dose
reconstruction, which have also been
promulgated by HHS as a final rule;
advice on the scientific validity and
quality of dose estimation and
reconstruction efforts being performed
for purposes of the compensation
program; and advice on petitions to add
classes of workers to the Special
Exposure Cohort (SEC).
In December 2000, the President
delegated responsibility for funding,
staffing, and operating the ABRWH to
HHS, which subsequently delegated this
authority to CDC. NIOSH implements
this responsibility for CDC. The charter
was issued on August 3, 2001, renewed
at appropriate intervals, and will expire
on August 3, 2011.
PURPOSE: The ABRWH is charged with
(a) Providing advice to the Secretary,
HHS, on the development of guidelines
under Executive Order 13179; (b)
providing advice to the Secretary, HHS,
on the scientific validity and quality of
dose reconstruction efforts performed
for this program; and (c) upon request
by the Secretary, HHS, advising the
Secretary on whether there is a class of
employees at any Department of Energy
facility who were exposed to radiation
but for whom it is not feasible to
estimate their radiation dose, and on
whether there is a reasonable likelihood
that such radiation doses may have
endangered the health of members of
this class. The Subcommittee on
Procedures Review was established to
aid the ABRWH in carrying out its duty
to advise the Secretary, HHS, on dose
reconstructions. The Subcommittee on
Procedures Review is responsible for
overseeing, tracking, and participating
in the reviews of all procedures used in
the dose reconstruction process by the
NIOSH Division of Compensation
Analysis and Support (DCAS) and its
dose reconstruction contractor.
MATTERS TO BE DISCUSSED: The agenda
for the Subcommittee meeting includes
discussion of the Norton Company
Special Exposure Cohort Petition (1962–
2009) and discussion of the following
ORAU and OCAS procedures: ORAUT–
RPRT–0044 (‘‘Analysis of Bioassay Data
with a Significant Fraction of Less-Than
Results’’), OCAS TIB–0013 (‘‘Special
External Dose Reconstruction
Considerations for Mallinckrodt
Workers’’), OTIB–019 (‘‘Analysis of
Coworker Bioassay Data for Internal
Dose Assignment’’), OTIB–0029
(‘‘Internal Dosimetry Coworker Data for
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38183
Y–12’’), OTIB–0047 (‘‘External
Radiation Monitoring at the Y–12
Facility During the 1948–1949 Period’’),
OTIB–0049 (‘‘Estimating Doses for
Plutonium Strongly Retained in the
Lung’’), OTIB–0052 (‘‘Parameters to
Consider When Processing Claims for
Construction Trade Workers’’), OTIB–
0054 (‘‘Fission and Activation Product
Assignment for Internal Dose-Related
Gross Beta and Gross Gamma
Analyses’’), and OTIB–0070 (‘‘Dose
Reconstruction During Residual
Radioactivity Periods at Atomic
Weapons Employer Facilities’’); and a
continuation of the comment-resolution
process for other dose reconstruction
procedures under review by the
Subcommittee.
The agenda is subject to change as
priorities dictate.
This meeting is open to the public,
but without a public comment period.
In the event an individual wishes to
provide comments, written comments
may be submitted. Any written
comments received will be provided at
the meeting and should be submitted to
the contact person below in advance of
the meeting.
CONTACT PERSON FOR MORE INFORMATION:
Theodore Katz, Executive Secretary,
NIOSH, CDC, 1600 Clifton Road,
Mailstop E–20, Atlanta, Georgia 30333,
Telephone (513)533–6800, Toll Free
1(800) CDC–INFO, E-mail
dcas@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.
Dated: June 23, 2011.
Elaine L. Baker,
Director, Management Analysis and Services
Office, Centers for Disease Control and
Prevention.
[FR Doc. 2011–16381 Filed 6–28–11; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Children and
Families
Agency Recordkeeping/Reporting
Requirements Under Emergency
Review by the Office of Management
and Budget (OMB)
Title: Evaluation of Adolescent
Pregnancy Prevention Approaches:
Baseline Data Collection.
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38184
Federal Register / Vol. 76, No. 125 / Wednesday, June 29, 2011 / Notices
OMB No.: 0970–0360.
Description: The Office of Adolescent
Health (OAH), Office of the Assistant
Secretary for Health (OASH), U.S.
Department of Health and Human
Services (HHS), is overseeing and
coordinating adolescent pregnancy
prevention evaluation efforts as part of
the Teen Pregnancy Prevention
Initiative. OAH is working
collaboratively with the Office of the
Assistant Secretary for Planning and
Evaluation (ASPE), the Centers for
Disease Control and Prevention (CDC),
and the Administration for Children and
Families (ACF) on adolescent pregnancy
prevention evaluation activities.
The Evaluation of Adolescent
Pregnancy Prevention Approaches
(PPA) is one of these efforts. PPA is a
random assignment evaluation which
will expand available evidence on
effective ways to reduce teen pregnancy.
The evaluation will document and test
a range of pregnancy prevention
approaches in up to eight program sites.
The findings from the evaluation will be
of interest to the general public, to
policy-makers, and to organizations
interested in teen pregnancy prevention.
OAH and ACF are proposing baseline
data collection activity as part of the
PPA evaluation. Baseline data collection
instruments were already approved on
July 26, 2010. The project has worked in
recent months to secure grantees as
evaluation sites, and as part of this effort
the project has undertaken making
revisions to the baseline instrument
with each site. These revisions were
undertaken because each site has
unique features (e.g. target population;
curriculum; objectives) and the baseline
instruments were tailored to take these
features into account. OAH and ACF are
now requesting emergency clearance to
collect data using site-specific
instruments.
Respondents will be asked to answer
carefully selected questions about
demographics and risk and protective
factors related to teen pregnancy.
Information from this data collection
will be used to perform meaningful
analysis to determine significant
program effects.
Respondents: The survey data will be
collected through private, selfadministered questionnaires completed
by study participants, i.e. adolescents
assigned to a select school or
community teen pregnancy prevention
program or a control group. Surveys will
be distributed and collected by trained
professional staff.
ANNUAL BURDEN ESTIMATES
Annualized no.
of respondents
Site/program (and name of baseline instrument)
No. of responses per
respondent
Average burden hours per
response
Total burden
hours
(annual)
Children’s Hospital of Los Angeles/Project AIM ..............................................
Oklahoma Institute of Child Advocacy/Power Through Choices .....................
Engender Health/Gender Matters ....................................................................
Ohio Health/T.O.P.P. .......................................................................................
Live the Life Ministries/WAIT Training .............................................................
Princeton Center for Leadership Training (PCLT)/TeenPEP ..........................
467
360
375
200
533
533
1
1
1
1
1
1
.7
.6
.6
.7
.7
.6
327
216
225
140
373
320
Total ..........................................................................................................
2468
........................
........................
1601
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Estimated Total Annual Burden
Hours: 1601.
Additional Information:
ACF is requesting that OMB grant a
180 day approval for this information
collection under procedures for
emergency processing by July 1, 2011. A
copy of this information collection, with
applicable supporting documentation,
may be obtained by e-mailing
OPREinfocollection@acf.hhs.gov.
Comments and questions about the
information collection described above
should be directed to the Office of
Information and Regulatory Affairs,
Attn: OMB Desk Officer for ACF, Office
of Management and Budget, Paperwork
Reduction Project, 725 17th Street NW.,
Washington, DC 20503, Fax (202) 395–
6974.
Robert Sargis,
Reports Clearance Officer.
[FR Doc. 2011–16290 Filed 6–28–11; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2011–N–0439]
Agency Information Collection
Activities; Proposed Collection;
Comment Request; FDA Recall
Regulations
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
the reporting requirements on FDA
recalls.
SUMMARY:
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Submit either electronic or
written comments on the collection of
information by August 29, 2011.
ADDRESSES: 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:
Daniel Gittleson, Office of Information
Management, Food and Drug
Administration, 1350 Piccard Dr. PI50–
400B, Rockville, MD 20850, 301–796–
5156, Daniel.Gittleson@fda.hhs.gov.
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
DATES:
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]]>Agencies
[Federal Register Volume 76, Number 125 (Wednesday, June 29, 2011)]
[Notices]
[Pages 38183-38184]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2011-16290]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Administration for Children and Families
Agency Recordkeeping/Reporting Requirements Under Emergency
Review by the Office of Management and Budget (OMB)
Title: Evaluation of Adolescent Pregnancy Prevention Approaches:
Baseline Data Collection.
[[Page 38184]]
OMB No.: 0970-0360.
Description: The Office of Adolescent Health (OAH), Office of the
Assistant Secretary for Health (OASH), U.S. Department of Health and
Human Services (HHS), is overseeing and coordinating adolescent
pregnancy prevention evaluation efforts as part of the Teen Pregnancy
Prevention Initiative. OAH is working collaboratively with the Office
of the Assistant Secretary for Planning and Evaluation (ASPE), the
Centers for Disease Control and Prevention (CDC), and the
Administration for Children and Families (ACF) on adolescent pregnancy
prevention evaluation activities.
The Evaluation of Adolescent Pregnancy Prevention Approaches (PPA)
is one of these efforts. PPA is a random assignment evaluation which
will expand available evidence on effective ways to reduce teen
pregnancy. The evaluation will document and test a range of pregnancy
prevention approaches in up to eight program sites. The findings from
the evaluation will be of interest to the general public, to policy-
makers, and to organizations interested in teen pregnancy prevention.
OAH and ACF are proposing baseline data collection activity as part
of the PPA evaluation. Baseline data collection instruments were
already approved on July 26, 2010. The project has worked in recent
months to secure grantees as evaluation sites, and as part of this
effort the project has undertaken making revisions to the baseline
instrument with each site. These revisions were undertaken because each
site has unique features (e.g. target population; curriculum;
objectives) and the baseline instruments were tailored to take these
features into account. OAH and ACF are now requesting emergency
clearance to collect data using site-specific instruments.
Respondents will be asked to answer carefully selected questions
about demographics and risk and protective factors related to teen
pregnancy. Information from this data collection will be used to
perform meaningful analysis to determine significant program effects.
Respondents: The survey data will be collected through private,
self-administered questionnaires completed by study participants, i.e.
adolescents assigned to a select school or community teen pregnancy
prevention program or a control group. Surveys will be distributed and
collected by trained professional staff.
Annual Burden Estimates
----------------------------------------------------------------------------------------------------------------
No. of Average burden
Site/program (and name of baseline instrument) Annualized no. responses per hours per Total burden
of respondents respondent response hours (annual)
----------------------------------------------------------------------------------------------------------------
Children's Hospital of Los Angeles/Project AIM.. 467 1 .7 327
Oklahoma Institute of Child Advocacy/Power 360 1 .6 216
Through Choices................................
Engender Health/Gender Matters.................. 375 1 .6 225
Ohio Health/T.O.P.P............................. 200 1 .7 140
Live the Life Ministries/WAIT Training.......... 533 1 .7 373
Princeton Center for Leadership Training (PCLT)/ 533 1 .6 320
TeenPEP........................................
---------------------------------------------------------------
Total....................................... 2468 .............. .............. 1601
----------------------------------------------------------------------------------------------------------------
Estimated Total Annual Burden Hours: 1601.
Additional Information:
ACF is requesting that OMB grant a 180 day approval for this
information collection under procedures for emergency processing by
July 1, 2011. A copy of this information collection, with applicable
supporting documentation, may be obtained by e-mailing
OPREinfocollection@acf.hhs.gov.
Comments and questions about the information collection described
above should be directed to the Office of Information and Regulatory
Affairs, Attn: OMB Desk Officer for ACF, Office of Management and
Budget, Paperwork Reduction Project, 725 17th Street NW., Washington,
DC 20503, Fax (202) 395-6974.
Robert Sargis,
Reports Clearance Officer.
[FR Doc. 2011-16290 Filed 6-28-11; 8:45 am]
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