Agency Information Collection Request. 60-Day Public Comment Request, 66102-66103 [2010-27137]
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66102
Federal Register / Vol. 75, No. 207 / Wednesday, October 27, 2010 / Notices
Desk Officer; faxed to OMB at 202–395–
5806.
Proposed Project: Family Planning
Annual Report: Forms and
Instructions—OMB No. 0990–0221—
Extension—Office of Population
Affairs—Title X Family Planning
Program.
Abstract: This request is for a 3-year
approval of the Family Planning Annual
service grantees, which include public
and private non-profit public heath
agencies. OPA uses FPAR data to
monitor compliance with statutory
requirements, to comply with
accountability and performance
requirements for GPRA and HHS plans,
and to guide program planning and
evaluation.
Report: Forms and Instructions (FPAR).
This is an annual reporting requirement
for family planning service delivery
projects authorized and funded under
the Population Research and Voluntary
Family Planning Programs (Section
1001 Title X of the Public Health
Service Act, 42 U.S.C. 300). The FPAR
is the only source of annual, uniform
reporting by all Title X family planning
ESTIMATED ANNUALIZED BURDEN TABLE
Forms
Type of
respondent
Number of
respondents
Number of
responses per
respondent
Average burden
(in hours) per
response
Total
burden
hours
FPAR: Forms and Instructions ...........
Title X service grantee .......................
88
1
40
3,520
Seleda Perryman,
Office of the Secretary, Paperwork Reduction
Act Clearance Officer.
[FR Doc. 2010–27136 Filed 10–26–10; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
[Document Identifier: OS–0990–0323; 60day Notice]
Agency Information Collection
Request. 60-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 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:
MedicalCountermeasures.gov.—OMB
No. 0990–0323—Extension—Office of
the Assistant Secretary for Preparedness
and Response (ASPR)—Office of the
Biomedical Advanced Research and
Development Authority (BARDA).
(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, e-mail your request,
including your address, phone number,
OMB number, and OS document
identifier, to
Sherette.funncoleman@hhs.gov, or call
the Reports Clearance Office at (202)
690–6162. Written comments and
recommendations for the proposed
information collections must be directed
to the OS Paperwork Clearance Officer
at the above e-mail address within 60
days.
Proposed Project: Meeting Request
Routing System for
Abstract: In order to route product
developers to the most appropriate
personnel within the Department of
Health and Human Services (HHS), HHS
collects some basic information about
the company’s product through
MedicalCountermeasures.gov. Using
this information and a routing system
that has been developed with input
from participating agencies within HHS,
including the Office of the Assistant
Secretary for Preparedness and
Response (ASPR), the Centers for
Disease Control and Prevention (CDC),
the Food and Drug Administration
(FDA), and the National Institutes of
Health (NIH),
MedicalCountermeasures.gov routes the
meeting request to the appropriate
person within HHS. ASPR is requesting
an extension by OMB for a three-year
clearance.
ESTIMATED ANNUALIZED BURDEN TABLE
Type of respondent
Number of
respondents
Number of
responses per
respondent
Average burden
(in hours) per
response
Total burden
hours
Meeting Request .....
srobinson on DSKHWCL6B1PROD with NOTICES
Forms
Medical Countermeasure Developers .......
225
1
8/60
30
Seleda M. Perryman,
Office of the Secretary, Paperwork Reduction
Act Clearance Officer.
[FR Doc. 2010–27137 Filed 10–26–10; 8:45 am]
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Federal Register / Vol. 75, No. 207 / Wednesday, October 27, 2010 / Notices
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2010–N–0544]
Agency Information Collection
Activities; Proposed Collection;
Comment Request; Application for
Participation in the Medical Device
Fellowship Program
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 application for participation in the
Medical Device Fellowship Program
(MDFP).
SUMMARY:
Submit either electronic or
written comments on the collection of
information by December 27, 2010.
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
DATES:
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 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
66103
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.
Application for Participation in the
Medical Device Fellowship Program—5
U.S.C. 1104, 1302, 3301, 3304, 3320,
3361, 3393, and 3394 (OMB Control
Number 0910–0551)—Extension
Sections 1104, 1302, 3301, 3304,
3320, 3361, 3393, and 3394 of Title 5 of
the United States Code, authorize
Federal agencies to rate applicants for
Federal jobs. Collecting applications for
the MDFP will allow FDA’s Center for
Devices and Radiological Health (CDRH)
to easily and efficiently elicit and
review information from students and
health care professionals who are
interested in becoming involved in
CDRH activities. The process will
reduce the time and cost of submitting
written documentation to the Agency
and lessen the likelihood of applications
being misrouted within the Agency mail
system. It will assist the Agency in
promoting and protecting the public
health by encouraging outside persons
to share their expertise with CDRH.
FDA estimates the burden of this
collection of information as follows:
TABLE 1—ESTIMATED ANNUAL REPORTING BURDEN 1
5 U.S.C. Section
FDA form No.
Number of
respondents
Annual
frequency per
response
Total annual
responses
Hours per
response
Total hours
1104, 1302, 3301, 3304, 3320, 3361,
3393, 3394 ...........................................
3608
250
1
250
1
250
1 There
are no capital costs or operating and maintenance costs associated with this collection of information.
FDA based these estimates on the
number of inquiries that have been
received concerning the program and
the number of requests for application
forms over the past 3 years.
Dated: October 21, 2010.
Leslie Kux,
Acting Assistant Commissioner for Policy.
[FR Doc. 2010–27158 Filed 10–26–10; 8:45 am]
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]]>Agencies
[Federal Register Volume 75, Number 207 (Wednesday, October 27, 2010)]
[Notices]
[Pages 66102-66103]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2010-27137]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
[Document Identifier: OS-0990-0323; 60-day Notice]
Agency Information Collection Request. 60-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 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.
To obtain copies of the supporting statement and any related forms
for the proposed paperwork collections referenced above, e-mail your
request, including your address, phone number, OMB number, and OS
document identifier, to Sherette.funncoleman@hhs.gov, or call the
Reports Clearance Office at (202) 690-6162. Written comments and
recommendations for the proposed information collections must be
directed to the OS Paperwork Clearance Officer at the above e-mail
address within 60 days.
Proposed Project: Meeting Request Routing System for
MedicalCountermeasures.gov.--OMB No. 0990-0323--Extension--Office of
the Assistant Secretary for Preparedness and Response (ASPR)--Office of
the Biomedical Advanced Research and Development Authority (BARDA).
Abstract: In order to route product developers to the most
appropriate personnel within the Department of Health and Human
Services (HHS), HHS collects some basic information about the company's
product through MedicalCountermeasures.gov. Using this information and
a routing system that has been developed with input from participating
agencies within HHS, including the Office of the Assistant Secretary
for Preparedness and Response (ASPR), the Centers for Disease Control
and Prevention (CDC), the Food and Drug Administration (FDA), and the
National Institutes of Health (NIH), MedicalCountermeasures.gov routes
the meeting request to the appropriate person within HHS. ASPR is
requesting an extension by OMB for a three-year clearance.
Estimated Annualized Burden Table
--------------------------------------------------------------------------------------------------------------------------------------------------------
Number of Average burden
Forms Type of respondent Number of responses per (in hours) per Total burden
respondents respondent response hours
--------------------------------------------------------------------------------------------------------------------------------------------------------
Meeting Request............................. Medical Countermeasure 225 1 8/60 30
Developers.
--------------------------------------------------------------------------------------------------------------------------------------------------------
Seleda M. Perryman,
Office of the Secretary, Paperwork Reduction Act Clearance Officer.
[FR Doc. 2010-27137 Filed 10-26-10; 8:45 am]
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