Agency Information Collection Activities: Submission for OMB Review; Comment Request, 80820 [2010-32196]
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80820
Federal Register / Vol. 75, No. 246 / Thursday, December 23, 2010 / Notices
the approximate time requested for the
presentation. Oral comments made at
the public meeting must also be
submitted to the NIOSH Docket Office
in writing in order to be considered by
the Agency.
Request for Information: NIOSH seeks
to obtain materials, including published
and unpublished reports and research
findings, to evaluate the possible health
risks of occupational exposure to carbon
nanotubes and nanofibers. Examples of
requested information include, but are
not to be limited to:
(1) Identification of industries or
occupations in which exposures to
carbon nanotubes and nanofibers can
occur;
(2) Trends in the production and use
of carbon nanotubes and nanofibers;
(3) Exposure measurement data;
(4) Case reports or other health
information demonstrating possible
health effects in workers exposed to
carbon nanotubes or nanofibers;
(5) Reports of experimental in vivo
and in vitro studies that provide
evidence of a dose-relationship between
exposure to carbon nanotubes and
nanofibers and biological activity;
(6) Reports of experimental data on
the airborne characteristics of carbon
nanotubes or nanofibers, including
information on the amounts that are
inhalable and respirable;
(7) Criteria and rationale for including
workers in a medical surveillance and
screening program;
(8) Description of work practices and
engineering controls used to reduce or
prevent workplace exposure to carbon
nanotubes and nanofibers; and
(9) Educational materials for worker
safety and training on the safe handling
of carbon nanotubes and nanofibers.
ADDRESSES: Written comments or
requests to attend or present at the
meeting, identified by docket number
NIOSH–161–A, may be submitted by
any of the following ways:
• Mail: NIOSH Docket Office, Robert
A. Taft Laboratories, MS–C34, 4676
Columbia Parkway, Cincinnati, OH
45226.
• Facsimile: (513) 533–8285.
• E-mail: nioshdocket@cdc.gov.
All information received in response
to this notice will be available for public
examination and copying at the NIOSH
Docket Office, 4676 Columbia Parkway,
Room 111, Cincinnati, OH 45226. A
complete electronic docket containing
all comments submitted will be
available on the NIOSH Web page at
https://www.cdc.gov/niosh/docket, and
comments will be available in writing
by request. NIOSH includes all
comments received without change in
VerDate Mar<15>2010
18:06 Dec 22, 2010
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the docket, including any personal
information provided. All electronic
comments should be formatted as
Microsoft Word. Please make reference
to docket number NIOSH 161–A.
FOR FURTHER INFORMATION CONTACT:
Ralph D. Zumwalde, NIOSH, Robert A.
Taft Laboratories MS–C32, 4676
Columbia Parkway, Cincinnati, OH
45226, telephone (513) 533–8320.
Dated: December 13, 2010.
Tanja Popovic,
Deputy Associate Director for Science,
Centers for Disease Control and Prevention.
[FR Doc. 2010–32328 Filed 12–22–10; 8:45 am]
BILLING CODE 4163–19–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[Document Identifier: CMS–R–153]
Agency Information Collection
Activities: Submission for OMB
Review; Comment Request
Centers for Medicare &
Medicaid Services, HHS.
In compliance with the requirement
of section 3506(c)(2)(A) of the
Paperwork Reduction Act of 1995, the
Centers for Medicare & Medicaid
Services (CMS), Department of Health
and Human Services, is publishing the
following summary of proposed
collections 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 function;
(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.
1. Type of Information Collection
Request: Reinstatement with change of a
previously approved collection; Title of
Information Collection: Medicaid Drug
Utilization Review (DUR) Annual
Report; Use: The DUR program is
required to assure that prescriptions are
appropriate, medically necessary and
are not likely to result in adverse
medical results. Each State DUR
program must consist of prospective
drug use review, retrospective drug use
review, data assessment of drug use
AGENCY:
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against predetermined standards, and
ongoing educational outreach activities.
In addition, States are required to
submit an annual DUR program report
that includes a description of the nature
and scope of State DUR activities. Over
the years, technology has changed as
has the practice of the pharmacy.
Therefore, CMS has revised the old
survey vehicle to more fully address the
current practices and areas of concern
with the Medicaid Pharmacy Programs.
Form Number: CMS–R–153 (OMB#:
0938–0659); Frequency: Annually;
Affected Public: State, Local, or Tribal
Governments; Number of Respondents:
51; Total Annual Responses: 51; Total
Annual Hours: 20,298. (For policy
questions regarding this collection
contact Madlyn Kruh at 410–786–3239.
For all other issues call 410–786–1326.)
To obtain copies of the supporting
statement and any related forms for the
proposed paperwork collections
referenced above, access CMS Web site
address at https://www.cms.hhs.gov/
PaperworkReductionActof1995,
or e-mail your request, including your
address, phone number, OMB number,
and CMS document identifier, to
Paperwork@cms.hhs.gov, or call the
Reports Clearance Office on (410) 786–
1326.
To be assured consideration,
comments and recommendations for the
proposed information collections must
be received by the OMB desk officer at
the address below, no later than 5 p.m.
on January 24, 2011: OMB, Office of
Information and Regulatory Affairs,
Attention: CMS Desk Officer. Fax
Number: (202) 395–6974. E-mail:
OIRA_submission@omb.eop.gov.
Dated: December 17, 2010.
Martique Jones,
Director, Regulations Development
Division-B, Office of Strategic Operations and
Regulatory Affairs.
[FR Doc. 2010–32196 Filed 12–22–10; 8:45 am]
BILLING CODE 4120–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[Document Identifier CMS–10367]
Agency Information Collection
Activities: Proposed Collection;
Comment Request
Centers for Medicare &
Medicaid Services, HHS.
In compliance with the requirement
of section 3506(c)(2)(A) of the
Paperwork Reduction Act of 1995, the
AGENCY:
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23DEN1
]]>Agencies
[Federal Register Volume 75, Number 246 (Thursday, December 23, 2010)]
[Notices]
[Page 80820]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2010-32196]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Medicare & Medicaid Services
[Document Identifier: CMS-R-153]
Agency Information Collection Activities: Submission for OMB
Review; Comment Request
AGENCY: Centers for Medicare & Medicaid Services, HHS.
In compliance with the requirement of section 3506(c)(2)(A) of the
Paperwork Reduction Act of 1995, the Centers for Medicare & Medicaid
Services (CMS), Department of Health and Human Services, is publishing
the following summary of proposed collections 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 function; (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.
1. Type of Information Collection Request: Reinstatement with
change of a previously approved collection; Title of Information
Collection: Medicaid Drug Utilization Review (DUR) Annual Report; Use:
The DUR program is required to assure that prescriptions are
appropriate, medically necessary and are not likely to result in
adverse medical results. Each State DUR program must consist of
prospective drug use review, retrospective drug use review, data
assessment of drug use against predetermined standards, and ongoing
educational outreach activities. In addition, States are required to
submit an annual DUR program report that includes a description of the
nature and scope of State DUR activities. Over the years, technology
has changed as has the practice of the pharmacy. Therefore, CMS has
revised the old survey vehicle to more fully address the current
practices and areas of concern with the Medicaid Pharmacy Programs.
Form Number: CMS-R-153 (OMB: 0938-0659); Frequency: Annually;
Affected Public: State, Local, or Tribal Governments; Number of
Respondents: 51; Total Annual Responses: 51; Total Annual Hours:
20,298. (For policy questions regarding this collection contact Madlyn
Kruh at 410-786-3239. For all other issues call 410-786-1326.)
To obtain copies of the supporting statement and any related forms
for the proposed paperwork collections referenced above, access CMS Web
site address at https://www.cms.hhs.gov/PaperworkReductionActof1995, or
e-mail your request, including your address, phone number, OMB number,
and CMS document identifier, to Paperwork@cms.hhs.gov, or call the
Reports Clearance Office on (410) 786-1326.
To be assured consideration, comments and recommendations for the
proposed information collections must be received by the OMB desk
officer at the address below, no later than 5 p.m. on January 24, 2011:
OMB, Office of Information and Regulatory Affairs, Attention: CMS Desk
Officer. Fax Number: (202) 395-6974. E-mail: OIRA_submission@omb.eop.gov.
Dated: December 17, 2010.
Martique Jones,
Director, Regulations Development Division-B, Office of Strategic
Operations and Regulatory Affairs.
[FR Doc. 2010-32196 Filed 12-22-10; 8:45 am]
BILLING CODE 4120-01-P
