Agency Information Collection Activities; Proposed Collection; Public Comment Request, 29370-29371 [2013-11949]
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29370
Federal Register / Vol. 78, No. 97 / Monday, May 20, 2013 / Notices
submitted to the Commission pursuant
to Subpart D of Part 14 of the
Commission’s rules or to any other
request by the Commission may be
submitted pursuant to a request for
confidentiality in accordance with 47
CFR 0.459 of the Commission’s rules.
Privacy Impact Assessment: The FCC
completed a Privacy Impact Assessment
(PIA) on June 28, 2007. The PIA may be
reviewed at https://www.fcc.gov/omd/
privacyact/
Privacy_Impact_Assessment.html. The
FCC is in the process of updating the
PIA to incorporate various revisions
made to the SORN.
Needs and Uses: On October 7, 2011,
in document FCC 11–151, the FCC
released a Report and Order adopting
final rules to implement sections 716
and 717 of the Communications Act of
1934 (the Act), as amended, which were
added to the Act by the Twenty-First
Century Communications and Video
Accessibility Act of 2010 (CVAA). See
Public Law 111–260, 104. Section 716 of
the Act requires providers of advanced
communications services and
manufacturers of equipment used for
advanced communications services to
make their services and equipment
accessible to individuals with
disabilities, unless doing so is not
achievable. 47 U.S.C. 617. Section 717
of the Act establishes new
recordkeeping requirements and
enforcement procedures for service
providers and equipment manufacturers
that are subject to sections 255, 716, and
718 of the Act. 47 U.S.C. 618. Section
255 of the Act requires
telecommunications and interconnected
VoIP services and equipment to be
accessible, if readily achievable. 47
U.S.C. 255. Section 718 of the Act
requires web browsers included on
mobile phones to be accessible to and
usable by individuals who are blind or
have a visual impairment, unless doing
so is not achievable. 47 U.S.C. 619.
Among other things, the FCC
established procedures in document
FCC 11–151 to facilitate the filing of
formal and informal complaints alleging
violations of sections 255, 716, or 718 of
the Act. Those procedures include a
nondiscretionary pre-filing notice
procedure to facilitate dispute
resolution. As a prerequisite to filing an
informal complaint, complainants must
first request dispute assistance from the
Consumer and Governmental Affairs
Bureau’s Disability Rights Office.
Pursuant to the new enforcement
rules that will go into effect on October
8, 2013, these informal complaints will
be filed on a new FCC Form 2000H. In
addition, a new Request for Dispute
Assistance form (FCC Form RDA) will
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be used to initiate the 30-day period
which must precede the filing of an
informal complaint. The burdens
associated with filing the new 2000H
and Request for Dispute Assistance
forms are contained in the collection
found in OMB control number 3060–
0874. Therefore, the Commission
extracted those burdens from the
collection found in OMB control
number 3060–1167. In addition, the
Commission has revised its estimate of
the number of requests for dispute
assistance and the number of informal
complaints that it expects to receive and
the burdens associated with the
processing and handling of those
requests and complaints.
Federal Communications Commission.
Gloria J. Miles,
Federal Register Liaison, Office of the
Secretary, Office of Managing Director.
[FR Doc. 2013–11879 Filed 5–17–13; 8:45 am]
BILLING CODE 6712–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Office of the Secretary
[Document Identifier: HHS–OS–19606–60D]
Agency Information Collection
Activities; Proposed Collection; Public
Comment Request
Office of the Secretary, HHS.
Notice.
AGENCY:
ACTION:
In compliance with section
3506(c)(2)(A) of the Paperwork
Reduction Act of 1995, the Office of the
Secretary (OS), Department of Health
and Human Services, announces plans
to submit an Information Collection
Request (ICR), described below, to the
Office of Management and Budget
(OMB). The ICR is for extending the use
of the approved information collection
assigned OMB control number 0990–
0221, which expires on January 31,
2014. Prior to submitting that ICR to
OMB, OS seeks comments from the
public regarding the burden estimate,
below, or any other aspect of the ICR.
DATES: Comments on the ICR must be
received on or before July 19, 2013.
ADDRESSES: Submit your comments to
Information.CollectionClearance@
hhs.gov or by calling (202) 690–6162.
FOR FURTHER INFORMATION CONTACT:
Information Collection Clearance staff,
Information.CollectionClearance@
hhs.gov or (202) 690–6162.
SUPPLEMENTARY INFORMATION: When
submitting comments or requesting
information, please include the
SUMMARY:
PO 00000
Frm 00053
Fmt 4703
Sfmt 4703
document identifier HHS–OS–19606–
60D for reference.
Information Collection Request Title:
Family Planning Annual Report: Forms
and Instructions
OMB No.: 0990–0221
Abstract: The Office of Population
Affairs (OPA), Office of the Assistant
Secretary for Health (OASH), U.S.
Department of Health and Human
Services (HHS) administers and
oversees the Title X Family Planning
Program. The Family Planning Annual
Report (FPAR) is an annual reporting
requirement for family planning
services delivery projects (‘‘Title X
service grantees’’) authorized and
funded by the Title X Family Planning
Program [‘‘Population Research and
Voluntary Family Planning Programs’’
(Pub. L. 91–572)], which was enacted in
1970 as Title X of the Public Health
Service Act (Section 1001 of Title X of
the Public Health Service Act, 42 United
States Code 300). The Title X Family
Planning Program is the only Federal
grant program dedicated solely to
providing individuals with
comprehensive family planning and
related preventive health services. The
program’s purpose is to assist
individuals in determining the number
and spacing of their children and is
designed to provide access to
contraceptive services, supplies, and
information to all who want and need
them. By law, priority is given to
persons from low-income families
(Section 1006[c] of 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 service
grantees. The FPAR provides consistent,
national-, regional-, state-, and granteelevel data on the services provided and
the characteristics of the individuals
served. Note that there are no changes
to the FPAR except minor corrections or
clarifications to submission and
reporting instructions or definitions.
The estimated average hour burden has
been reduced to 36 hours, which is 4
hours lower than the 40-hour estimate
of the previous OMB submission.
Need and Proposed Use of the
Information: OPA uses FPAR data to
monitor compliance with statutory
requirements and accountability and
federal performance requirements for
Title X family planning funds as
required by the 1993 Government
Performance and Results Act (GPRA)
and HHS, to guide financial and
program planning and evaluation, and
to respond to inquiries about the
program from policymakers and
Congress.
Likely Respondents: Title X service
grantees.
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Federal Register / Vol. 78, No. 97 / Monday, May 20, 2013 / Notices
technology and systems for the purpose
of collecting, validating and verifying
information, processing and
maintaining information, and disclosing
and providing information, to train
personnel and to be able to respond to
a collection of information, to search
Burden Statement: Burden in this
context means the time expended by
persons to generate, maintain, retain,
disclose, or provide the information
requested. This includes the time
needed to review instructions, to
develop, acquire, install and utilize
data sources, to complete and review
the collection of information, and to
transmit or otherwise disclose the
information. The total annual burden
hours estimated for this ICR are
summarized in the table below.
TOTAL ESTIMATED ANNUALIZED BURDEN-HOURS
Number of
respondents
Form name
Number of
responses per
respondent
Average
burden per
response
(in hours)
Total burden
hours
Family Planning Annual Report: Forms and Instructions ................................
93
1
36
3,348
Total ..........................................................................................................
93
1
36
3,348
OS specifically requests comments on
(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.
Keith A. Tucker,
Information Collection Clearance Officer.
[FR Doc. 2013–11949 Filed 5–17–13; 8:45 am]
BILLING CODE 4150–28–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Informational Meeting Concerning
Compliance With the Centers for
Disease Control and Prevention’s
Import Permit Program; Public
Webcast
Centers for Disease Control and
Prevention (CDC), Department of Health
and Human Services (HHS).
ACTION: Notice of public webcast.
AGENCY:
The Centers for Disease
Control and Prevention (CDC),
Department of Health and Human
Services (HHS) announces a public
webcast that will address the new
import permit regulations for infectious
biological agents, standards, and
vectors; import permit inspections; and
import permit exemptions. The purpose
of this notice is to inform all interested
parties, including those individuals and
entities already possessing an import
permit of the webcast.
DATES: The webcast will be held on
Friday, July 12, 2013 from 1 p.m. to 5
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On
February 4, 2013, the Centers for
Disease Control and Prevention (CDC) in
the Department of Health and Human
Services (HHS) published a final rule
(78 FR 7674) amending etiological
importation regulations to (1) clarify
import permit regulatory definitions, (2)
increase oversight by implementing
inspections, (3) address exemptions and
(4) describe the appeal process.
This webcast is an opportunity for the
regulated community (i.e., academic
institutions and biomedical centers,
commercial manufacturing facilities,
federal, state, and local laboratories,
including clinical and diagnostic
laboratories, research facilities,
exhibition facilities, and educational
facilities) and other interested
individuals to obtain specific regulatory
guidance and information regarding the
newly amended regulations. The
webcast will also provide assistance to
those interested in applying for an
etiological agent import permit.
Representatives from HHS/CDC will be
present during the webcast to address
questions and concerns from the web
participants.
SUPPLEMENTARY INFORMATION:
Centers for Disease Control and
Prevention
SUMMARY:
p.m. EST. Those wishing to join the
webcast are encouraged to register by
July 5, 2013. Registration instructions
are found on the HHS/CDC’s Import
Permit Program Web site, https://
www.cdc.gov/od/eaipp/index.htm.
ADDRESSES: The webcast will be
broadcast from the Centers for Disease
Control and Prevention, 1600 Clifton
Road NE., Atlanta, Georgia 30329.
FOR FURTHER INFORMATION CONTACT: Von
McClee, Division of Select Agents and
Toxins, Office of Public Health
Preparedness and Response, Centers for
Disease Control and Prevention, 1600
Clifton Road NE., MS A–46, Atlanta, GA
30333; phone: 404–718–2000; email:
lrsat@cdc.gov.
PO 00000
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Fmt 4703
Sfmt 4703
Topics to be discussed during the
webcast include: The new import
permit regulations for infectious
biological agents, standards, and
vectors; import permit inspections; and
import permit exemptions. A question
and answer session will take place after
each topic.
Individuals wishing to join the
webcast are encouraged to register by
July 5, 2013. Instructions for registration
are found on the HHS/CDC’s Import
Permit Program Web site, https://
www.cdc.gov/od/eaipp/index.htm. This
is a webcast only event and there will
be no on-site participation at the HHS/
CDC broadcast facility. In-person
participation cannot be accommodated.
Closed-captioning video of the webcast
will be available at https://www.cdc.gov/
od/eaipp/index.htm after the webcast.
Dated: May 14, 2013.
Tanja Popovic,
Deputy Associate Director for Science,
Centers for Disease Control and Prevention.
[FR Doc. 2013–11895 Filed 5–17–13; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
Eunice Kennedy Shriver National
Institute of Child Health & Human
Development; Notice of Closed
Meetings
Pursuant to section 10(d) of the
Federal Advisory Committee Act, as
amended (5 U.S.C. App.), notice is
hereby given of the following meeting.
The meeting will be closed to the
public in accordance with the
provisions set forth in sections
552b(c)(4) and 552b(c)(6), Title 5 U.S.C.,
as amended. The grant applications and
the discussions could disclose
confidential trade secrets or commercial
E:\FR\FM\20MYN1.SGM
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]]>Agencies
[Federal Register Volume 78, Number 97 (Monday, May 20, 2013)]
[Notices]
[Pages 29370-29371]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2013-11949]
=======================================================================
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Office of the Secretary
[Document Identifier: HHS-OS-19606-60D]
Agency Information Collection Activities; Proposed Collection;
Public Comment Request
AGENCY: Office of the Secretary, HHS.
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: In compliance with section 3506(c)(2)(A) of the Paperwork
Reduction Act of 1995, the Office of the Secretary (OS), Department of
Health and Human Services, announces plans to submit an Information
Collection Request (ICR), described below, to the Office of Management
and Budget (OMB). The ICR is for extending the use of the approved
information collection assigned OMB control number 0990-0221, which
expires on January 31, 2014. Prior to submitting that ICR to OMB, OS
seeks comments from the public regarding the burden estimate, below, or
any other aspect of the ICR.
DATES: Comments on the ICR must be received on or before July 19, 2013.
ADDRESSES: Submit your comments to
Information.CollectionClearance@hhs.gov or by calling (202) 690-6162.
FOR FURTHER INFORMATION CONTACT: Information Collection Clearance
staff, Information.CollectionClearance@hhs.gov or (202) 690-6162.
SUPPLEMENTARY INFORMATION: When submitting comments or requesting
information, please include the document identifier HHS-OS-19606-60D
for reference.
Information Collection Request Title: Family Planning Annual
Report: Forms and Instructions
OMB No.: 0990-0221
Abstract: The Office of Population Affairs (OPA), Office of the
Assistant Secretary for Health (OASH), U.S. Department of Health and
Human Services (HHS) administers and oversees the Title X Family
Planning Program. The Family Planning Annual Report (FPAR) is an annual
reporting requirement for family planning services delivery projects
(``Title X service grantees'') authorized and funded by the Title X
Family Planning Program [``Population Research and Voluntary Family
Planning Programs'' (Pub. L. 91-572)], which was enacted in 1970 as
Title X of the Public Health Service Act (Section 1001 of Title X of
the Public Health Service Act, 42 United States Code 300). The Title X
Family Planning Program is the only Federal grant program dedicated
solely to providing individuals with comprehensive family planning and
related preventive health services. The program's purpose is to assist
individuals in determining the number and spacing of their children and
is designed to provide access to contraceptive services, supplies, and
information to all who want and need them. By law, priority is given to
persons from low-income families (Section 1006[c] of 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 service grantees. The FPAR
provides consistent, national-, regional-, state-, and grantee-level
data on the services provided and the characteristics of the
individuals served. Note that there are no changes to the FPAR except
minor corrections or clarifications to submission and reporting
instructions or definitions. The estimated average hour burden has been
reduced to 36 hours, which is 4 hours lower than the 40-hour estimate
of the previous OMB submission.
Need and Proposed Use of the Information: OPA uses FPAR data to
monitor compliance with statutory requirements and accountability and
federal performance requirements for Title X family planning funds as
required by the 1993 Government Performance and Results Act (GPRA) and
HHS, to guide financial and program planning and evaluation, and to
respond to inquiries about the program from policymakers and Congress.
Likely Respondents: Title X service grantees.
[[Page 29371]]
Burden Statement: Burden in this context means the time expended by
persons to generate, maintain, retain, disclose, or provide the
information requested. This includes the time needed to review
instructions, to develop, acquire, install and utilize technology and
systems for the purpose of collecting, validating and verifying
information, processing and maintaining information, and disclosing and
providing information, to train personnel and to be able to respond to
a collection of information, to search data sources, to complete and
review the collection of information, and to transmit or otherwise
disclose the information. The total annual burden hours estimated for
this ICR are summarized in the table below.
Total Estimated Annualized Burden-Hours
----------------------------------------------------------------------------------------------------------------
Average
Number of Number of burden per Total burden
Form name respondents responses per response (in hours
respondent hours)
----------------------------------------------------------------------------------------------------------------
Family Planning Annual Report: Forms and 93 1 36 3,348
Instructions...................................
---------------------------------------------------------------
Total....................................... 93 1 36 3,348
----------------------------------------------------------------------------------------------------------------
OS specifically requests comments on (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.
Keith A. Tucker,
Information Collection Clearance Officer.
[FR Doc. 2013-11949 Filed 5-17-13; 8:45 am]
BILLING CODE 4150-28-P
