Agency Information Collection Activities: Proposed Collection; Comment Request, 38297-38298 [2012-15694]
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Federal Register / Vol. 77, No. 124 / Wednesday, June 27, 2012 / Notices
HHS/CDC has posted the original
notice and all related materials on
www.regulations.gov.
Dated: June 20, 2012.
Kathleen Sebelius,
Secretary, Department of Health and Human
Services.
[FR Doc. 2012–15642 Filed 6–26–12; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Disease Control and
Prevention
[Docket Number NIOSH–033–A]
Revised Document Posted: NIOSH List
of Antineoplastic and Other Hazardous
Drugs in Healthcare Settings 2012
National Institute for
Occupational Safety and Health
(NIOSH) of the Centers for Disease
Control and Prevention (CDC),
Department of Health and Human
Services (HHS).
ACTION: Notice of issuance of Final
Guidance Publication.
AGENCY:
srobinson on DSK4SPTVN1PROD with NOTICES
Dated: June 20, 2012.
John Howard,
Director, National Institute for Occupational
Safety and Health, Centers for Disease Control
and Prevention.
[FR Doc. 2012–15651 Filed 6–26–12; 8:45 am]
The National Institute for
Occupational Safety and Health
(NIOSH) of the Centers for Disease
Control and Prevention (CDC)
announces the publication of the
following document entitled ‘‘NIOSH
List of Antineoplastic and Other
Hazardous Drugs in Healthcare Settings
2012.’’ NIOSH is making available a
copy of Appendix A at https://
www.cdc.gov/niosh/docs/2012-150.
Background: The NIOSH Alert:
NIOSH published Preventing
Occupational Exposures to
Antineoplastic and Other Hazardous
Drugs in Health Care Settings in
September 2004 (https://www.cdc.gov/
niosh/docs/2004-165/). Appendix A of
this Alert defined hazardous drugs and
provided a list of drugs that were
considered hazardous and required
special handling. In 2010, NIOSH
published an update to this list
(https://www.cdc.gov/niosh/docs/2010167/). Since publishing the 2010 update
to the list, NIOSH reviewed
approximately 70 new drugs that
received FDA approval and
approximately 180 drugs that received
new special warnings (usually black box
warnings) based on reported adverse
effects in patients covering the time
period from October 2007 to December
2009. From this list of approximately
250 drugs, NIOSH determined 26 drugs
to have one or more characteristics of a
hazardous drug. In addition, NIOSH
removed 15 drugs from the 2012 list
SUMMARY:
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19:05 Jun 26, 2012
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because they did not meet the NIOSH
definition, were no longer available in
the U.S or were regulated by other
government entities. NIOSH published
this preliminary list for comment in
NIOSH Docket Number 190.
After expert panel review, public
review and comment, and review of the
scientific literature, NIOSH has
developed a revised list of hazardous
drugs. Along with drugs initially
identified in the 2010 Hazardous Drug
List, NIOSH is adding a total of 26 new
drugs to the 2012 NIOSH List of
Hazardous Drugs and is deleting 15
drugs.
This guidance document does not
have the force and effect of law.
FOR FURTHER INFORMATION CONTACT:
Barbara MacKenzie, NIOSH, Robert A.
Taft Laboratories, 4676 Columbia
Parkway, MS–C26, Cincinnati, OH
45226, Telephone (513) 533–8132, email
hazardousdrugs@cdc.gov.
BILLING CODE 4163–19–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[Document Identifier CMS–359 and –360]
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
Centers for Medicare & Medicaid
Services (CMS) 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 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.
AGENCY:
PO 00000
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38297
1. Type of Information Collection
Request: Extension without change of a
currently approved collection. Title of
Information Collection: Comprehensive
Outpatient Rehabilitation Facility
(CORF) Eligibility and Survey Forms.
Use: CMS–359 serves as the application
for facilities wishing to participate in
the Medicare/Medicaid program as
CORFs. The form initiates the process
for obtaining a decision as to whether
the conditions of participation are met.
It also promotes data reduction (key
punching) or introduction to and
retrieval from the Medicare/Medicaid
Automated Certification System,
ASPEN, by the CMS Regional Offices
(ROs). Should any question arise
regarding the structure of the
organization, this information is readily
available without going through the
process of completing the form again.
CMS–360 is used by the State survey
agency to record data collected to
determine provider compliance with
individual conditions of participation
and to report it to the Federal
government. CMS has the responsibility
and authority for certification decisions
which are based on provider
compliance with the conditions of
participation. The information needed
to make these decisions is available to
CMS only through use of information
abstracted from the survey checklists.
The form is primarily a worksheet
designed to facilitate keypunching into
the ASPEN by the State Agency after the
survey is completed.
Form Number: CMS–359 (CORF
Eligibility Form) and CMS–360 (CORF
Survey Report Form); OCN 0938–0267.
Frequency: Occasionally. Affected
Public: Private Sector (Business or other
for-profits). Number of Respondents:
295. Total Annual Responses: 42. Total
Annual Hours: 137. (For policy
questions regarding this collection
contact Georgia Johnson at 410–786–
6859. 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
Email 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.
In commenting on the proposed
information collections please reference
the document identifier or OMB control
number. To be assured consideration,
comments and recommendations must
E:\FR\FM\27JNN1.SGM
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38298
Federal Register / Vol. 77, No. 124 / Wednesday, June 27, 2012 / Notices
be submitted in one of the following
ways by August 27, 2012:
1. Electronically. You may submit
your comments electronically to https://
www.regulations.gov. Follow the
instructions for ‘‘Comment or
Submission’’ or ‘‘More Search Options’’
to find the information collection
document(s) accepting comments.
2. By regular mail. You may mail
written comments to the following
address: CMS, Office of Strategic
Operations and Regulatory Affairs,
Division of Regulations Development,
Attention: Document Identifier/OMB
Control Number lllll, Room C4–
26–05, 7500 Security Boulevard,
Baltimore, Maryland 21244–1850.
Dated: June 22, 2012.
Martique Jones,
Director, Regulations Development Group,
Division B, Office of Strategic Operations and
Regulatory Affairs.
[FR Doc. 2012–15694 Filed 6–26–12; 8:45 am]
BILLING CODE 4120–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[Document Identifier CMS–10429]
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: New collection (request for a
new OMB control number). Title of
Information Collection: Surveys of
Physicians and Home Health Agencies
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to Assess Access Issues for Specific
Medicare Beneficiaries as Defined in
Section 3131(d) of the ACA. Use: This
collection is part of a study called for
under section 3131(d) of the Patient
Protection and Affordable Care Act
(ACA). The study is focused on two
major issues: (1) supporting CMS’ efforts
to improve payment accuracy and (2)
understanding issues of access for the
ACA populations under the existing
home health prospective payment
system. The study team’s analytic plan
focuses on understanding payment
accuracy for the specific study
populations through claims and cost
data analyses, which will reflect
payments and costs for patients who
have gained access to home health care.
In order to understand access issues for
the ACA defined populations, the study
team proposes using survey instruments
to better understand the characteristics
of Medicare beneficiaries who are not
able to gain access to or have
experienced delays in gaining access to
home health services.
As a new collection, the information
collected is expected to support CMS’
efforts to improve the home health
prospective payment system payment
accuracy for vulnerable populations and
thereby ensure the payment system does
not inadvertently cause avoidable access
problems. The questions are designed to
provide insights into access issues for
vulnerable populations that cannot be
learned through analyses of
administrative data.
Form Number: CMS–10429 (OCN:
0938–New). Frequency: Once. Affected
Public: Private Sector (business or other
for-profit and not-for-profit institutions).
Number of Respondents: 875. Total
Annual Responses: 292. Total Annual
Hours: 73. (For policy questions
regarding this collection contact Kristy
Chu at 410–786–8953. 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
Email 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 July 27, 2012. OMB, Office of
Information and Regulatory Affairs,
Attention: CMS Desk Officer, Fax
PO 00000
Frm 00032
Fmt 4703
Sfmt 4703
Number: (202) 395–6974, Email:
OIRA_submission@omb.eop.gov.
Dated: June 22, 2012.
Martique Jones,
Director, Regulations Development Group,
Division-B, Office of Strategic Operations and
Regulatory Affairs.
[FR Doc. 2012–15693 Filed 6–26–12; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Children and
Families
Submission for OMB Review;
Comment Request
Title: Parents and Children Together.
OMB No.: 0970–0403.
Description: The Administration for
Children and Families (ACF), U.S.
Department of Health and Human
Services is proposing an information
collection activity as part of an
evaluation of healthy marriage and
responsible fatherhood grant programs.
The evaluation study title is Parents and
Children Together (PACT).
A 60-Day Federal Register Notice was
published for this study on December
20, 2011. This Notice described all
components of the study and, therefore,
we request to waive additional 60-Day
Federal Register Notices. This 30-Day
Federal Register Notice covers (a)
instruments for the impact study
baseline survey (including an
introductory script and the baseline
survey itself), and (b) site Management
Information Systems (MIS).
This information collection request is
specific to Responsible Fatherhood
programs that may be evaluated
(requests specific to Healthy Marriage
programs will be separate). The baseline
survey will collect data related to such
domains as father involvement,
coparenting, parenting, marriage and
romantic relationships, and
employment. The information from the
baseline survey will be used by ACF for,
among other things, describing the
populations served and determining the
comparability of program and control
groups. Information on participant
entry, participation, and exit from the
program will be entered into the MIS
system.
Respondents: Baseline information
will be collected from all fathers prior
to random assignment; the introductory
script will be read by program staff to
fathers applying to the program.
Program staff will record information on
the services received by study
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Agencies
[Federal Register Volume 77, Number 124 (Wednesday, June 27, 2012)]
[Notices]
[Pages 38297-38298]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2012-15694]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Medicare & Medicaid Services
[Document Identifier CMS-359 and -360]
Agency Information Collection Activities: Proposed Collection;
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) 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 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.
1. Type of Information Collection Request: Extension without change
of a currently approved collection. Title of Information Collection:
Comprehensive Outpatient Rehabilitation Facility (CORF) Eligibility and
Survey Forms. Use: CMS-359 serves as the application for facilities
wishing to participate in the Medicare/Medicaid program as CORFs. The
form initiates the process for obtaining a decision as to whether the
conditions of participation are met. It also promotes data reduction
(key punching) or introduction to and retrieval from the Medicare/
Medicaid Automated Certification System, ASPEN, by the CMS Regional
Offices (ROs). Should any question arise regarding the structure of the
organization, this information is readily available without going
through the process of completing the form again.
CMS-360 is used by the State survey agency to record data collected
to determine provider compliance with individual conditions of
participation and to report it to the Federal government. CMS has the
responsibility and authority for certification decisions which are
based on provider compliance with the conditions of participation. The
information needed to make these decisions is available to CMS only
through use of information abstracted from the survey checklists. The
form is primarily a worksheet designed to facilitate keypunching into
the ASPEN by the State Agency after the survey is completed.
Form Number: CMS-359 (CORF Eligibility Form) and CMS-360 (CORF
Survey Report Form); OCN 0938-0267. Frequency: Occasionally. Affected
Public: Private Sector (Business or other for-profits). Number of
Respondents: 295. Total Annual Responses: 42. Total Annual Hours: 137.
(For policy questions regarding this collection contact Georgia Johnson
at 410-786-6859. 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 Email 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.
In commenting on the proposed information collections please
reference the document identifier or OMB control number. To be assured
consideration, comments and recommendations must
[[Page 38298]]
be submitted in one of the following ways by August 27, 2012:
1. Electronically. You may submit your comments electronically to
https://www.regulations.gov. Follow the instructions for ``Comment or
Submission'' or ``More Search Options'' to find the information
collection document(s) accepting comments.
2. By regular mail. You may mail written comments to the following
address: CMS, Office of Strategic Operations and Regulatory Affairs,
Division of Regulations Development, Attention: Document Identifier/OMB
Control Number ----------, Room C4-26-05, 7500 Security Boulevard,
Baltimore, Maryland 21244-1850.
Dated: June 22, 2012.
Martique Jones,
Director, Regulations Development Group, Division B, Office of
Strategic Operations and Regulatory Affairs.
[FR Doc. 2012-15694 Filed 6-26-12; 8:45 am]
BILLING CODE 4120-01-P