Agency Information Collection Request; 30-Day Public Comment Request, 37046-37047 [2012-15033]
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37046
Federal Register / Vol. 77, No. 119 / Wednesday, June 20, 2012 / Notices
processes for reviewing the applications
and awarding grant funds. These
processes are reflected in agencies’
policies and procedures documents.
Agencies will also maintain and store
application forms and data in
accordance with their policies and
practices.
The 4040–0003 collection expired on
November 30, 2011. The Grants.gov
Program Management Office requests a
reinstatement without change.
ESTIMATED ANNUALIZED BURDEN TABLE
Number of
annual
respondents
Number of
responses per
respondent
Average
burden on
respondent
per response
in hours
Form
Type of
respondent
SF–424 Short, Project Abstract, and
Key Contacts Forms (4040–0003).
Grant Applicant ................................
13,615
1
1
13,615
Total ...........................................
...........................................................
13,615
1
1
13,615
Keith A. Tucker,
Office of the Secretary, Paperwork Reduction
Act Clearance Officer.
[FR Doc. 2012–15028 Filed 6–19–12; 8:45 am]
BILLING CODE 4151–AE–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
[Document Identifier: OS–0990–0279; 30day Notice]
Agency Information Collection
Request; 30-Day Public Comment
Request
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, is
publishing the following summary of a
proposed collection 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
AGENCY:
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. Send written comments and
recommendations for the proposed
information collections within 30 days
of this notice directly to the OS OMB
Desk Officer; faxed to OMB at 202–395–
5806.
Proposed Project: Institutional Review
Board Form—Extension—OMB No.
0990–0279—Office for Human Research
Protections
Total burden
hours
Abstract: The Office for Human
Research Protections (OHRP) and the
Food and Drug Administration (FDA)
are requesting a three-year extension of
the OMB No. 0990–0279, Institutional
Review Board (IRB) Registration Form.
This form was modified in 2009 to be
consistent with IRB registration
requirements that were adopted in July
2009 by OHRP and FDA, respectively.
Respondents for this information
collection are institutions or
organizations operating IRBs designated
by an institution under an assurance of
compliance approved for federalwide
use by OHRP under 45 CFR 46.103(a)
and that review human subjects
research conducted or supported by
HHS, or, in the case of FDA’s regulation,
each IRB in the United States that
reviews clinical investigations regulated
by FDA under sections 505(i) or 520(g)
of the Federal Food, Drug and Cosmetic
Act; and each IRB in the United States
that reviews clinical investigations that
are intended to support applications for
research or marketing permits for FDAregulated products.
TOTAL ESTIMATED ANNUALIZED BURDEN—HOURS
Number of
respondents
Form name
Number of
responses per
respondent
Average
burden per
response
(in hours)
Total burden
hours
6,100
900
2
2
1
1
12,200
1,800
Total ..........................................................................................................
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Already Registered IRBs .................................................................................
New IRBs .........................................................................................................
........................
........................
........................
14,000
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37047
Federal Register / Vol. 77, No. 119 / Wednesday, June 20, 2012 / Notices
Keith A. Tucker,
Paperwork Reduction Act Reports Clearance
Officer, Office of the Secretary.
[FR Doc. 2012–15033 Filed 6–19–12; 8:45 am]
BILLING CODE 4150–36–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
[Document Identifier: OS–0990–New; 60-day
Notice]
Agency Information Collection
Request; 60-Day Public Comment
Request
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, 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.
AGENCY:
baseline capacity for clinical laboratory
information exchange.
The National Survey on Health
Information Exchange in Clinical
Laboratories will assess and evaluate
the electronic transfer of health
information from clinical laboratories to
ordering physicians. It will focus on two
key measures: (1) Percentage of
laboratory facilities that are able to send
structured lab results electronically to
ordering physicians and (2) Percentage
of lab results that are currently begin
sent electronically in coded format to
ordering physicians.
The anticipated bi-annual data
collection effort will be conducted in
two waves—Wave I in November of
2012 will establish the baseline and
Wave II in 2014 will measure progress.
Information will be collected using a
mail-out/mail-back hard copy
questionnaire with telephone nonresponse follow up. There will be two
similar versions of the questionnaire—
one for hospital-based labs and one for
independent labs. For hospitals, the
burden hours are based on an estimated
length of approximately 20 minutes per
completed survey. ONC will use these
survey findings to develop a
comprehensive understanding of the
baseline level of laboratory information
exchange in order to inform program
activities to promote laboratory
information exchange and provide more
targeted assistance to states and
territories in developing their laboratory
information exchange strategies.
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)
690–6162. 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: National Survey on
Health Information Exchange in Clinical
Laboratories OMB No. 0090–NEW—
Office of the National Coordinator for
Health Information Technology.
Abstract: Currently, the Office of the
National Coordinator for Health
Information Technology (ONC) is
soliciting comments on a new
information collection activity that will
collect key data from a relatively small
sample of clinical laboratories
nationwide for the Evaluation of the
State Health Information Exchange
Cooperative Agreement Program. A key
goal of the State Health Information
Exchange Cooperative Agreement
Program is to promote the electronic
exchange of structured test results from
clinical laboratories to healthcare
providers. To assess progress over time
at both the national and state level,
information is needed regarding the
ESTIMATED ANNUALIZED BURDEN TABLE
Average
burden
(in hours)
per response
Type of
respondent
Hospital-Based Laboratory Survey on
Health Information Exchange.
Independent Laboratory Survey on Health
Information Exchange.
Hospital-Based Laboratories
2,882
1
20/60
961
Independent Laboratories .....
2,081
1
17.57/60
609
...............................................
4,963
1
18.98/60
1,570
Total .......................................................
Number of
respondents
Number of
responses per
respondent
Forms
Keith A. Tucker,
Office of the Secretary, Paperwork Reduction
Act Clearance Officer.
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
[FR Doc. 2012–15032 Filed 6–19–12; 8:45 am]
Agency for Healthcare Research and
Quality
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BILLING CODE 4150–36–P
Agency Information Collection
Activities; Proposed Collection;
Comment Request
Agency for Healthcare Research
and Quality, HHS.
AGENCY:
ACTION:
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Total burden
hours
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:
‘‘Synthesis of AHRQ-Funded HAI
Projects.’’ In accordance with the
Paperwork Reduction Act, 44 U.S.C.
3501–3521, AHRQ invites the public to
comment on this proposed information
collection.
This proposed information collection
was previously published in the Federal
SUMMARY:
E:\FR\FM\20JNN1.SGM
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]]>Agencies
[Federal Register Volume 77, Number 119 (Wednesday, June 20, 2012)]
[Notices]
[Pages 37046-37047]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2012-15033]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
[Document Identifier: OS-0990-0279; 30-day Notice]
Agency Information Collection Request; 30-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, is publishing the following
summary of a proposed collection 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. Send written comments and
recommendations for the proposed information collections within 30 days
of this notice directly to the OS OMB Desk Officer; faxed to OMB at
202-395-5806.
Proposed Project: Institutional Review Board Form--Extension--OMB
No. 0990-0279--Office for Human Research Protections
Abstract: The Office for Human Research Protections (OHRP) and the
Food and Drug Administration (FDA) are requesting a three-year
extension of the OMB No. 0990-0279, Institutional Review Board (IRB)
Registration Form. This form was modified in 2009 to be consistent with
IRB registration requirements that were adopted in July 2009 by OHRP
and FDA, respectively. Respondents for this information collection are
institutions or organizations operating IRBs designated by an
institution under an assurance of compliance approved for federalwide
use by OHRP under 45 CFR 46.103(a) and that review human subjects
research conducted or supported by HHS, or, in the case of FDA's
regulation, each IRB in the United States that reviews clinical
investigations regulated by FDA under sections 505(i) or 520(g) of the
Federal Food, Drug and Cosmetic Act; and each IRB in the United States
that reviews clinical investigations that are intended to support
applications for research or marketing permits for FDA-regulated
products.
Total Estimated Annualized Burden--Hours
----------------------------------------------------------------------------------------------------------------
Average
Number of Number of burden per Total burden
Form name respondents responses per response (in hours
respondent hours)
----------------------------------------------------------------------------------------------------------------
Already Registered IRBs......................... 6,100 2 1 12,200
New IRBs........................................ 900 2 1 1,800
---------------------------------------------------------------
Total....................................... .............. .............. .............. 14,000
----------------------------------------------------------------------------------------------------------------
[[Page 37047]]
Keith A. Tucker,
Paperwork Reduction Act Reports Clearance Officer, Office of the
Secretary.
[FR Doc. 2012-15033 Filed 6-19-12; 8:45 am]
BILLING CODE 4150-36-P
