Proposed Information Collection Activity; Comment Request, 75180 [05-24174]
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75180
Federal Register / Vol. 70, No. 242 / Monday, December 19, 2005 / Notices
Control System, Medicare contractors
and the Coordination of Benefit
Contractor, Common Working File, CMS
Regional Offices, an agency of a State
government, Medicare beneficiaries and
non-Medicare beneficiaries that have an
approved or denied WC Medicare Setaside arrangement to cover future
medical costs resulting from an injury
incurred while employed and the Social
Security Administration.
SYSTEMS EXEMPTED FROM CERTAIN PROVISION
OF THE ACT:
None.
[FR Doc. E5–7486 Filed 12–16–05; 8:45 am]
BILLING CODE 4120–03–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Children and
Families
Proposed Information Collection
Activity; Comment Request
Proposed Projects
Title: Sanction Policies Task Order.
OMB No.: New Collection.
Description: This study is designed to
determine how local welfare offices
implement sanction policies in the
Temporary Assistance for Needy
Families program. This study will
survey local welfare staff to gather indepth qualitative information on how
workers interpret the policies and apply
them in specific instances. The results
of this study should give the
Administration for Children and
Families (ACF) a better understanding
of possible outcomes of various sanction
policies, which in turn will help ACF
design a research program to study the
effect of sanctions.
Respondents: A maximum of 324
welfare staff in local welfare offices.
ANNUAL BURDEN ESTIMATES
Instrument
Number of
respondents
Number of
responses
per respondent
Average
burden
hours per response
Total burden
hours
In-person Survey and Telephone Interviews ...................................................
324
1
.85
275
Estimated Total Annual Burden
Hours: 275.
In compliance with the requirements
of section 3506(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.
VerDate Aug<31>2005
18:59 Dec 16, 2005
Jkt 208001
Dated: December 12, 2005.
Robert Sargis,
Reports Clearance Officer.
[FR Doc. 05–24174 Filed 12–16–05; 8:45 am]
BILLING CODE 4184–01–M
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. 1980N–0208]
Biological Products; Bacterial
Vaccines and Toxoids; Implementation
of Efficacy Review; Anthrax Vaccine
Adsorbed; Final Order
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice.
Frm 00032
Fmt 4703
The final order on categorization
of AVA is effective December 19, 2005.
FOR FURTHER INFORMATION CONTACT:
Kathleen Swisher, Center for Biologics
Evaluation and Research (HFM–17),
Food and Drug Administration, 1401
Rockville Pike, Suite 200N, Rockville,
MD 20852–1448, 301–827–6210.
SUPPLEMENTARY INFORMATION:
DATES:
Table of Contents
The Food and Drug
Administration (FDA) proposed, among
other things, to classify Anthrax Vaccine
Adsorbed (AVA) on the basis of findings
and recommendations of the Panel on
Review of Bacterial Vaccines and
Toxoids (the Panel) on December 13,
1985. The Panel reviewed the safety,
efficacy, and labeling of bacterial
vaccines and toxoids with standards of
potency, bacterial antitoxins, and
immune globulins. After the initial final
rule and final order was vacated by the
United States District Court for the
District of Columbia on October 27,
2004, FDA published a new proposed
rule and proposed order on December
29, 2004. The purpose of this final order
is to categorize AVA according to the
evidence of its safety and effectiveness,
SUMMARY:
PO 00000
thereby determining if it may remain
licensed and on the market; issue a final
response to recommendations made in
the Panel’s report, and; respond to
comments on the previously published
proposed order. The final rule and final
order concerning bacterial vaccines and
toxoids other than AVA is published
elsewhere in this issue of the Federal
Register.
Sfmt 4703
I. Introduction
II. Background
A. General Description of the
‘‘Efficacy Review’’ for Biological
Products Licensed Before July 1972
B. The December 1985 Proposal
C. Additional Proceedings Following
the December 1985 Proposal
III. Categorization of Anthrax Vaccine
Adsorbed—Final Order
A. Efficacy of Anthrax Vaccine
Adsorbed
B. Safety of Anthrax Vaccine
Adsorbed
C. The Panel’s General Statement:
Anthrax Vaccine, Adsorbed,
Description of Product
D. The Panel’s Specific Product
E:\FR\FM\19DEN1.SGM
19DEN1
]]>Agencies
[Federal Register Volume 70, Number 242 (Monday, December 19, 2005)]
[Notices]
[Page 75180]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 05-24174]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Administration for Children and Families
Proposed Information Collection Activity; Comment Request
Proposed Projects
Title: Sanction Policies Task Order.
OMB No.: New Collection.
Description: This study is designed to determine how local welfare
offices implement sanction policies in the Temporary Assistance for
Needy Families program. This study will survey local welfare staff to
gather in-depth qualitative information on how workers interpret the
policies and apply them in specific instances. The results of this
study should give the Administration for Children and Families (ACF) a
better understanding of possible outcomes of various sanction policies,
which in turn will help ACF design a research program to study the
effect of sanctions.
Respondents: A maximum of 324 welfare staff in local welfare
offices.
Annual Burden Estimates
----------------------------------------------------------------------------------------------------------------
Number of Average burden
Instrument Number of responses per hours per Total burden
respondents respondent response hours
----------------------------------------------------------------------------------------------------------------
In-person Survey and Telephone Interviews... 324 1 .85 275
----------------------------------------------------------------------------------------------------------------
Estimated Total Annual Burden Hours: 275.
In compliance with the requirements of section 3506(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: December 12, 2005.
Robert Sargis,
Reports Clearance Officer.
[FR Doc. 05-24174 Filed 12-16-05; 8:45 am]
BILLING CODE 4184-01-M
