Proposed Information Collection Activity; Comment Request, 6400-6401 [2010-2761]
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Federal Register / Vol. 75, No. 26 / Tuesday, February 9, 2010 / Notices
safety, permanency, and well-being for
children, youth, and families. The
Children’s Bureau desires to assess the
quality and effectiveness of the
technical assistance it supports, and
several of these programs and projects
are required to be evaluated, including
those funded under Section 105 of The
Child Abuse Prevention and Treatment
Act, as amended [42 U.S.C. 5106].
Beginning in fiscal year (FY) 2010, the
T/TA Network will comprise a group of
30 T/TA providers funded entirely or
partially by the Children’s Bureau
through grants, contracts, and
interagency agreements.
The cross-site evaluation uses a
mixed-method, longitudinal approach to
examine the ICs (funded in FY 2009)
and a new cohort of NRCs (funded in FY
2010). Proposed data collection methods
are a longitudinal telephone survey of
State child welfare directors (or their
designees) and Tribal Child Welfare/
Social Service Directors (or their
designees), a Web-based survey of State
and Tribal T/TA recipients, and
aggregation of outputs from a Web-based
technical assistance tracking system
(OneNet) that will be used by the five
ICs and 11 NRCs. A Web-based survey
will be also administered to members of
the T/TA Network. Data collected
through these instruments will be used
by the Children’s Bureau to evaluate the
effectiveness of technical assistance
delivered to State, local, Tribal, and
other publicly administered or publicly
supported child welfare agencies and
family and juvenile courts and the
overall functioning of the T/TA
Network.
Respondents: Respondents to two of
the survey instruments will be State and
Tribal governments. Respondents to the
third survey will be private institutions,
including universities, not-for-profit
organizations, and private companies.
Private institutions, including
universities and not-for-profit
organizations will be respondents to the
forms in the OneNet tracking system.
ANNUAL BURDEN ESTIMATES
Number of
respondents
Instrument
Cprice-sewell on DSK2BSOYB1PROD with NOTICES
OneNet Form: General T/TA Event .................................................................
OneNet Form: NRC T/TA Work Plan ..............................................................
OneNet Form: NRC T/TA Close-Out ...............................................................
OneNet Form: NRC T/TA Activity ....................................................................
OneNet Form: Implementation Project Monthly Report ..................................
Agency Results Survey ...................................................................................
Training and Technical Assistance (T/TA) Activity Survey .............................
Web-Based Network Survey ............................................................................
OneNet Form: Implementation Project Information .........................................
OneNet Form: Implementation Project T/TA Activity ......................................
Estimated Total Annual Burden
Hours: 2,135.56.
Additional Information:
Copies of the proposed collection may
be obtained by writing to the
Administration for Children and
Families, Office of Administration,
Office of Information Services, 370
L’Enfant Promenade, SW., Washington,
DC 20447, Attn: ACF Reports Clearance
Officer. All requests should be
identified by the title of the information
collection. E-mail 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
16
11
11
11
5
74
160
30
5
5
directly to the following: Office of
Management and Budget, Paperwork
Reduction Project, Fax: 202–395–7245,
Attn: Desk Officer for the
Administration for Children and
Families.
Dated: February 4, 2010.
Robert Sargis,
Reports Clearance Officer.
[FR Doc. 2010–2804 Filed 2–8–10; 8:45 am]
BILLING CODE 4184–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Children and
Families
Proposed Information Collection
Activity; Comment Request
Number of
responses per
respondent
26
45
45
528
62.40
1
3
1
5.40
280.80
Average
burden hours
per response
0.25
0.20
0.08
0.20
0.17
1
0.25
0.25
0.50
0.33
Total
burden hours
104
99
39.60
1,161.60
53.04
74
120
7.50
13.50
463.32
OMB No.: 0970–0323.
Description: The Improper Payments
Information Act of 2002 requires
Federal agencies to annually report error
rate measures. Section 2 of the Improper
Payments Information Act provides for
estimates and reports of improper
payments by Federal agencies. Subpart
K of 45 CFR, Part 98 requires
preparation and submission of a report
of errors occurring in the administration
of CCDF grant funds once every three
years. The information collected will be
used to prepare the annual Agency
Financial Report (AFR) and will provide
information necessary to offer technical
assistance to grantees.
Respondents: State grantees, the
District of Columbia, and Puerto Rico.
Proposed Projects
Title: CCDF—Reporting Improper
Payments—Instructions for States.
ANNUAL BURDEN ESTIMATES
Number of
respondents
Instrument
OMB #0970–0323 Record Review Worksheet ................................................
OMB #0970–0323 Data Entry Form ................................................................
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17
Number of
responses per
respondent
276.38
276.38
E:\FR\FM\09FEN1.SGM
09FEN1
Average
burden hours
per response
15.43
0.18
Total
burden hours
72,497.24
845.72
6401
Federal Register / Vol. 75, No. 26 / Tuesday, February 9, 2010 / Notices
ANNUAL BURDEN ESTIMATES—Continued
Number of respondents
Instrument
Number of responses per
respondent
Average burden hours per
response
17
1
639
OMB #0970–0323 State Improper Authorizations for Payment Report ..........
Estimated Total Annual Burden
Hours: 84,205.96
In compliance with the requirements
of Section 506(c)(2)(A) of the Paperwork
Reduction Act of 1995, the
Administration for Children and
Families is soliciting public comment
on the specific aspects of the
information collection described above.
Copies of the proposed collection of
information can be obtained and
comments may be forwarded by writing
to the Administration for Children and
Families, Office of Administration,
Office of Information Services, 370
L’Enfant Promenade, SW., Washington,
DC 20447, Attn: ACF Reports Clearance
Officer. E-mail address:
infocollection@acf.hhs.gov. All requests
should be identified by the title of the
information collection.
The Department specifically requests
comments on: (a) Whether the proposed
collection of information is necessary
for the proper performance of the
functions of the agency, including
whether the information shall have
practical utility; (b) the accuracy of the
agency’s estimate of the burden of the
proposed collection of information; (c)
the quality, utility, and clarity of the
information to be collected; and (d)
ways to minimize the burden of the
collection of information on
respondents, including through the use
of automated collection techniques or
other forms of information technology.
Consideration will be given to
comments and suggestions submitted
within 60 days of this publication.
Dated: February 4, 2010.
Robert Sargis,
Reports Clearance Officer.
[FR Doc. 2010–2761 Filed 2–8–10; 8:45 am]
Food and Drug Administration
[Docket No. FDA–2009–M–0513]
Medical Devices Regulated by the
Center for Biologics Evaluation and
Research; Availability of Summaries of
Safety and Effectiveness Data for
Premarket Approval Applications
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice.
SUMMARY: The Food and Drug
Administration (FDA) is publishing a
list of premarket approval applications
(PMAs) that have been approved by the
Center for Biologics Evaluation and
Research (CBER). This list is intended to
inform the public of the availability
through the Internet and FDA’s Division
of Dockets Management of summaries of
safety and effectiveness data of
approved PMAs.
ADDRESSES: Submit written requests for
copies of summaries of safety and
effectiveness data to the Division of
Dockets Management (HFA–305), Food
and Drug Administration, 5630 Fishers
Lane, rm. 1061, Rockville, MD 20852.
Please include the appropriate docket
number as listed in table 1 of this
document when submitting a written
request. See the SUPPLEMENTARY
INFORMATION section for electronic
access to the summaries of safety and
effectiveness data.
FOR FURTHER INFORMATION CONTACT:
Melissa Reisman, Center for Biologics
Evaluation and Research (HFM–17),
Food and Drug Administration, suite
200N, 1401 Rockville Pike, Rockville,
MD 20852–1448, 301–827–6210.
SUPPLEMENTARY INFORMATION:
I. Background
In the Federal Register of January 30,
1998 (63 FR 4571), FDA published a
final rule that revised 21 CFR 814.44(d)
BILLING CODE 4184–01–P
Cprice-sewell on DSK2BSOYB1PROD with NOTICES
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Total burden
hours
10,863
and 814.45(d) to discontinue individual
publication of PMA approvals and
denials in the Federal Register,
providing instead to post this
information on the Internet at https://
www.fda.gov. In addition, the
regulations provide that FDA publish a
quarterly list of available safety and
effectiveness summaries of PMA
approvals and denials that were
announced during the quarter. FDA
believes that this procedure expedites
public notification of these actions
because announcements can be placed
on the Internet more quickly than they
can be published in the Federal
Register, and FDA believes that the
Internet is accessible to more people
than the Federal Register.
In accordance with section 515(d)(4)
and (e)(2) of the Federal Food, Drug, and
Cosmetic Act (the act) (21 U.S.C.
360e(d)(4) and (e)(2)), notification of an
order approving, denying, or
withdrawing approval of a PMA will
continue to include a notice of
opportunity to request review of the
order under section 515(g) of the act.
The 30-day period for requesting
administrative reconsideration of an
FDA action under § 10.33(b) (21 CFR
10.33(b)) for notices announcing
approval of a PMA begins on the day the
notice is placed on the Internet. Section
10.33(b) provides that FDA may, for
good cause, extend this 30-day period.
Reconsideration of a denial or
withdrawal of approval of a PMA may
be sought only by the applicant; in these
cases, the 30-day period will begin
when the applicant is notified by FDA
in writing of its decision.
The following is a list of PMAs
approved by CBER for which summaries
of safety and effectiveness data were
placed on the Internet from July 1, 2009,
through September 30, 2009. There were
no denial actions during this period.
The list provides the manufacturer’s
name, the product’s generic name or the
trade name, and the approval date.
TABLE 1.—LIST OF SUMMARIES OF SAFETY AND EFFECTIVENESS DATA FOR APPROVED PMAS MADE AVAILABLE JULY 1,
2009, THROUGH SEPTEMBER 30, 2009.
PMA No./Docket No.
BP090022/0/
FDA–2009–M–0513
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TRADE NAME
Approval Date
Avioq HIV–1 Microelisa System
September 21, 2009
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]]>Agencies
[Federal Register Volume 75, Number 26 (Tuesday, February 9, 2010)]
[Notices]
[Pages 6400-6401]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2010-2761]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Administration for Children and Families
Proposed Information Collection Activity; Comment Request
Proposed Projects
Title: CCDF--Reporting Improper Payments--Instructions for States.
OMB No.: 0970-0323.
Description: The Improper Payments Information Act of 2002 requires
Federal agencies to annually report error rate measures. Section 2 of
the Improper Payments Information Act provides for estimates and
reports of improper payments by Federal agencies. Subpart K of 45 CFR,
Part 98 requires preparation and submission of a report of errors
occurring in the administration of CCDF grant funds once every three
years. The information collected will be used to prepare the annual
Agency Financial Report (AFR) and will provide information necessary to
offer technical assistance to grantees.
Respondents: State grantees, the District of Columbia, and Puerto
Rico.
Annual Burden Estimates
----------------------------------------------------------------------------------------------------------------
Number of Average burden
Instrument Number of responses per hours per Total burden
respondents respondent response hours
----------------------------------------------------------------------------------------------------------------
OMB 0970-0323 Record Review Worksheet.. 17 276.38 15.43 72,497.24
OMB 0970-0323 Data Entry Form.......... 17 276.38 0.18 845.72
[[Page 6401]]
OMB 0970-0323 State Improper 17 1 639 10,863
Authorizations for Payment Report..............
----------------------------------------------------------------------------------------------------------------
Estimated Total Annual Burden Hours: 84,205.96
In compliance with the requirements of Section 506(c)(2)(A) of the
Paperwork Reduction Act of 1995, the Administration for Children and
Families is soliciting public comment on the specific aspects of the
information collection described above. Copies of the proposed
collection of information can be obtained and comments may be forwarded
by writing to the Administration for Children and Families, Office of
Administration, Office of Information Services, 370 L'Enfant Promenade,
SW., Washington, DC 20447, Attn: ACF Reports Clearance Officer. E-mail
address: infocollection@acf.hhs.gov. All requests should be identified
by the title of the information collection.
The Department specifically requests comments on: (a) Whether the
proposed collection of information is necessary for the proper
performance of the functions of the agency, including whether the
information shall have practical utility; (b) the accuracy of the
agency's estimate of the burden of the proposed collection of
information; (c) the quality, utility, and clarity of the information
to be collected; and (d) ways to minimize the burden of the collection
of information on respondents, including through the use of automated
collection techniques or other forms of information technology.
Consideration will be given to comments and suggestions submitted
within 60 days of this publication.
Dated: February 4, 2010.
Robert Sargis,
Reports Clearance Officer.
[FR Doc. 2010-2761 Filed 2-8-10; 8:45 am]
BILLING CODE 4184-01-P
