Submission for OMB Review; Comment Request, 6820-6821 [2013-02079]
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6820
Federal Register / Vol. 78, No. 21 / Thursday, January 31, 2013 / Notices
PSO. Accordingly, The Connecticut
Hospital Association Federal Patient
Safety Organization was delisted
effective at 12:00 Midnight ET (2400) on
December 1, 2012.
More information on PSOs can be
obtained through AHRQ’s PSO Web site
at https://www.pso.AHRQ.gov/
index.html.
Dated: January 17, 2O13.
Carolyn M. Clancy,
Director.
[FR Doc. 2013–01919 Filed 1–30–13; 8:45 am]
BILLING CODE 4160–90–M
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Agency for Healthcare Research and
Quality
Patient Safety Organizations:
Voluntary Relinquishment From Ryder
Trauma Center
Agency for Healthcare Research
and Quality (AHRQ), HHS.
ACTION: Notice of delisting.
AGENCY:
The Patient Safety and
Quality Improvement Act of 2005
(Patient Safety Act), Public Law 109–41,
42 U.S.C. 299b–21—b–26, provides for
the formation of Patient Safety
Organizations (PSOs), which collect,
aggregate, and analyze confidential
information regarding the quality and
safety of health care delivery. The
Patient Safety and Quality Improvement
Final Rule (Patient Safety Rule), 42 CFR
Part 3, authorizes AHRQ, on behalf of
the Secretary of HHS, to list as a PSO
an entity that attests that it meets the
statutory and regulatory requirements
for listing. A PSO can be ‘‘delisted’’ by
the Secretary if it is found no longer to
meet the requirements of the Patient
Safety Act and Patient Safety Rule, or
when a PSO chooses to voluntarily
relinquish its status as a PSO for any
reason. AHRQ has accepted a
notification of voluntary relinquishment
from Ryder Trauma Center of its status
SUMMARY:
as a PSO, and has delisted the PSO
accordingly.
DATES: The directories for both listed
and delisted PSOs are ongoing and
reviewed weekly by AHRQ. The
delisting was effective at 12:00 Midnight
ET (2400) on November 20, 2012.
ADDRESSES: Both directories can be
accessed electronically at the following
HHS Web site: https://
www.pso.AHRQ.gov/.
FOR FURTHER INFORMATION CONTACT:
Eileen Hogan, Center for Quality
Improvement and Patient Safety, AHRQ,
540 Gaither Road, Rockville, MD 20850;
Telephone (toll free): (866) 403–3697;
Telephone (local): (301) 427–1111; TTY
(toll free): (866) 438–7231; TTY (local):
(301) 427–1130; Email:
pso@AHRQ.hhs.gov.
SUPPLEMENTARY INFORMATION:
Jackson Memorial Hospital, to
voluntarily relinquish its status as a
PSO. Accordingly, Ryder Trauma Center
was delisted effective at 12:00 Midnight
ET (2400) on November 20, 2012.
More information on PSOs can be
obtained through AHRQ’s PSO Web site
at https://www.pso.AHRQ.gov/
index.html.
Background
The Patient Safety Act authorizes the
listing of PSOs, which are entities or
component organizations whose
mission and primary activity is to
conduct activities to improve patient
safety and the quality of health care
delivery.
HHS issued the Patient Safety Rule to
implement the Patient Safety Act.
AHRQ administers the provisions of the
Patient Safety Act and Patient Safety
Rule (PDF file, 450 KB. PDF Help)
relating to the listing and operation of
PSOs.
The Patient Safety Rule authorizes
AHRQ to list as a PSO an entity that
attests that it meets the statutory and
regulatory requirements for listing. A
PSO can be ‘‘delisted’’ if it is found no
longer to meet the requirements of the
Patient Safety Act and Patient Safety
Rule, or when a PSO chooses to
voluntarily relinquish its status as a
PSO for any reason. Section 3.108(d) of
the Patient Safety Rule requires AHRQ
to provide public notice when it
removes an organization from the list of
federally approved PSOs.
AHRQ has accepted a notification
from Ryder Trauma Center, PSO number
P0019, which is a component entity of
Submission for OMB Review;
Comment Request
Dated: January 17, 2013.
Carolyn M. Clancy,
Director.
[FR Doc. 2013–01909 Filed 1–30–13; 8:45 am]
BILLING CODE 4160–90–M
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Children and
Families
Title: Child Care and Development
Fund Annual Financial Report (ACF–
696T) for Tribes.
OMB No.: 0970–0195.
Description: Tribes use the Financial
Report Form ACF–696T to report Child
Care and Development Fund (CCDF)
expenditures. Authority to collect and
report this information is found in
Section 658G of the Child Care and
Development Block Grant Act of 1990,
as revised. In addition to the Program
Reporting Requirements set forth in 45
CFR part 98, subpart H, the regulations
at 45 CFR 98.65(g) and 98.67(c)(1)
authorize the Secretary to require
financial reports as necessary.
Tribal grantees submit the ACF–696T
report on an annual basis on behalf of
the Tribal Lead Agency administering
the Child Care and Development Fund
(CCDF).
The previous information collection
requirements related to the American
Recovery and Reinvestment Act (ARRA)
of 2009 (Pub. L. 111–5) have been
deleted from this reporting form.
Respondents: Tribes and Tribal
Organizations that are CCDF grantees.
ANNUAL BURDEN ESTIMATES
Number of
respondents
Number of
responses per
respondent
Estimated
average
burden hours
per response
Estimated total
burden hours
ACF–696T CCDF Financial Reporting Form for Tribes ..................................
srobinson on DSK4SPTVN1PROD with
Instrument
260
1
6
1560
Estimated Total Annual Burden
Hours: 1560.
Additional Information: Copies of the
proposed collection may be obtained by
VerDate Mar<15>2010
17:38 Jan 30, 2013
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writing to the Administration for
Children and Families, Office of
Planning, Research and Evaluation, 370
PO 00000
Frm 00018
Fmt 4703
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L’Enfant Promenade SW., Washington,
DC 20447, Attn: ACF Reports Clearance
Officer. All requests should be
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6821
Federal Register / Vol. 78, No. 21 / Thursday, January 31, 2013 / Notices
identified by the title of the information
collection. Email address:
infocollection@acf.hhs.gov.
OMB Comment: OMB is required to
make a decision concerning the
collection of information between 30
and 60 days after publication of this
document in the Federal Register.
Therefore, a comment is best assured of
having its full effect if OMB receives it
within 30 days of publication. Written
comments and recommendations for the
proposed information collection should
be sent directly to the following: Office
of Management and Budget, Paperwork
Reduction Project, Fax: 202–395–7285,
Email: OIRA_SUBMISSION@OMB.EOP.
GOV, Attn: Desk Officer for the
Administration for Children and
Families.
Robert Sargis,
Reports Clearance Officer.
[FR Doc. 2013–02079 Filed 1–30–13; 8:45 am]
BILLING CODE 4184–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Notice.
[Docket No. FDA–2012–N–0427]
Agency Information Collection
Activities; Submission for Office of
Management and Budget Review;
Comment Request; Medical Devices;
Inspection by Accredited Persons
Program
Food and Drug Administration,
Inspection by Accredited Persons
Program Under the Medical Device
User Fee and Modernization Act of
2002—(OMB Control Number 0910–
0510)—Extension
The Food and Drug
Administration (FDA) is announcing
that a proposed collection of
information has been submitted to the
Office of Management and Budget
(OMB) for review and clearance under
the Paperwork Reduction Act of 1995.
SUMMARY:
Fax written comments on the
collection of information by March 4,
2013.
DATES:
To ensure that comments on
the information collection are received,
OMB recommends that written
comments be faxed to the Office of
Information and Regulatory Affairs,
OMB, Attn: FDA Desk Officer, FAX:
202–395–7285, or emailed to
oira_submission@omb.eop.gov. All
comments should be identified with the
OMB control number 0910–0510. Also
include the FDA docket number found
in brackets in the heading of this
document.
ADDRESSES:
FOR FURTHER INFORMATION CONTACT:
Food and Drug Administration
AGENCY:
ACTION:
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.
In
compliance with 44 U.S.C. 3507, FDA
has submitted the following proposed
collection of information to OMB for
review and clearance.
SUPPLEMENTARY INFORMATION:
HHS.
The Medical Device User Fee and
Modernization Act of 2002 (MDUFMA)
(Pub. L. 107–250) was signed into law
on October 26, 2002. Section 201 of
MDUFMA adds a new paragraph (g) to
section 704 of the Federal, Food, Drug,
and Cosmetic Act (the FD&C Act) (21
U.S.C. 374), directing FDA to accredit
third parties (accredited persons) to
conduct inspections of eligible
manufacturers of class II or class III
devices. This is a voluntary program.
FDA has a guidance document that
provides information for those
interested in participating in this
program. The guidance is entitled
‘‘Implementation of the Inspection by
Accredited Persons Program Under the
Medical Device User Fee and
Modernization Act of 2002;
Accreditation Criteria.’’
FDA based these estimates on
conversations with industry, trade
association representatives, and internal
FDA estimates. Once an organization is
accredited, it will not be required to
reapply.
In the Federal Register of May 09,
2012 (77 FR 27234), FDA published a
60-day notice requesting public
comment on the proposed collection of
information. No comments were
received.
FDA estimates the burden of this
collection of information as follows:
TABLE 1.—ESTIMATED ANNUAL REPORTING BURDEN 1
Number of
responses per
respondent
Number of
respondents
Average
burden per
response
Total annual
responses
Section of the FD&C Act
Activity
704(g) ..................................
Request for accreditation ...
1
1
1
80
80
Total .............................
.............................................
........................
........................
........................
........................
80
srobinson on DSK4SPTVN1PROD with
1 There
are no capital costs or operating and maintenance costs associated with this collection of information.
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Total hours
]]>Agencies
[Federal Register Volume 78, Number 21 (Thursday, January 31, 2013)]
[Notices]
[Pages 6820-6821]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2013-02079]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Administration for Children and Families
Submission for OMB Review; Comment Request
Title: Child Care and Development Fund Annual Financial Report
(ACF-696T) for Tribes.
OMB No.: 0970-0195.
Description: Tribes use the Financial Report Form ACF-696T to
report Child Care and Development Fund (CCDF) expenditures. Authority
to collect and report this information is found in Section 658G of the
Child Care and Development Block Grant Act of 1990, as revised. In
addition to the Program Reporting Requirements set forth in 45 CFR part
98, subpart H, the regulations at 45 CFR 98.65(g) and 98.67(c)(1)
authorize the Secretary to require financial reports as necessary.
Tribal grantees submit the ACF-696T report on an annual basis on
behalf of the Tribal Lead Agency administering the Child Care and
Development Fund (CCDF).
The previous information collection requirements related to the
American Recovery and Reinvestment Act (ARRA) of 2009 (Pub. L. 111-5)
have been deleted from this reporting form.
Respondents: Tribes and Tribal Organizations that are CCDF
grantees.
Annual Burden Estimates
----------------------------------------------------------------------------------------------------------------
Estimated
Number of Number of average burden Estimated total
Instrument respondents responses per hours per burden hours
respondent response
----------------------------------------------------------------------------------------------------------------
ACF-696T CCDF Financial Reporting Form for 260 1 6 1560
Tribes.....................................
----------------------------------------------------------------------------------------------------------------
Estimated Total Annual Burden Hours: 1560.
Additional Information: Copies of the proposed collection may be
obtained by writing to the Administration for Children and Families,
Office of Planning, Research and Evaluation, 370 L'Enfant Promenade
SW., Washington, DC 20447, Attn: ACF Reports Clearance Officer. All
requests should be
[[Page 6821]]
identified by the title of the information collection. Email address:
infocollection@acf.hhs.gov.
OMB Comment: OMB is required to make a decision concerning the
collection of information between 30 and 60 days after publication of
this document in the Federal Register. Therefore, a comment is best
assured of having its full effect if OMB receives it within 30 days of
publication. Written comments and recommendations for the proposed
information collection should be sent directly to the following: Office
of Management and Budget, Paperwork Reduction Project, Fax: 202-395-
7285, Email: OIRA_SUBMISSION@OMB.EOP.GOV, Attn: Desk Officer for the
Administration for Children and Families.
Robert Sargis,
Reports Clearance Officer.
[FR Doc. 2013-02079 Filed 1-30-13; 8:45 am]
BILLING CODE 4184-01-P
