Agency Information Collection Activities: Submission for OMB Review; Comment Request, 57744-57745 [2011-23807]
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57744
Federal Register / Vol. 76, No. 180 / Friday, September 16, 2011 / Notices
Instructions for Submitting an
Intervention
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
To submit an intervention,
individuals should send a written
statement to NREPP expressing their
interest along with documentation that
demonstrates the intervention meets the
minimum requirements as described
above. All submissions must be made
either by a principal investigator (PI)
who has conducted research on the
intervention, a project director (PD) who
has worked with an evaluator of the
intervention, or a formally authorized
delegate of the PI or PD. For information
on where to submit materials, please
call 1–866–436–7377. Electronic
submissions are preferred, but materials
may be sent to NREPP in hard copy via
postal mail or fax. To be eligible for
consideration, submissions must be
received no later than 11:59 p.m. E.S.T.
on February 1, 2012; those received
before November 1, 2011, will be
disregarded.
For each intervention that is accepted,
the Principal (the individual, usually
the PI, formally designated as the
intervention’s point of contact and
decisionmaking authority during the
review process) will be asked to submit
additional documentation to be used in
the review. This additional
documentation includes full-text copies
of all articles and reports that provide
evidence of significant outcomes
(p ≤ .05) as well as copies of selected
dissemination materials in the format
they are provided to the public (e.g.,
hard copies or electronic versions of
manuals, training presentations, tools,
quality assurance protocols; URLs for
interactive Web-based resources).
The Principal continues to work with
NREPP staff throughout the review and
is responsible for approval of the final
intervention summary that is developed
by NREPP staff once the review has
been completed.
Centers for Disease Control and
Prevention
Contact Information
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Individuals who have questions about
the information contained in this notice
may write to NREPP staff at
nrepp@samhsa.hhs.gov or call 1–866–
436–7377.
[FR Doc. 2011–23757 Filed 9–15–11; 8:45 am]
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Advisory Committee to the Director
(ACD), Centers for Disease Control and
Prevention (CDC)—Ethics
Subcommittee (ES)
Correction: This notice was published
in the Federal Register on September 8,
2011, Volume 76, Number 174, Page
55678. The correct time should be 1
p.m.–3:30 p.m.
Contact Person for More Information:
Drue Barrett, Ph.D., Designated Federal
Officer, ACD, CDC—ES, CDC, 1600
Clifton Road, NE., M/S D–50, Atlanta,
Georgia 30333. Telephone (404) 639–
4690. E-mail: dbarrett@cdc.gov.
The Director, Management Analysis
and Services Office, has been delegated
the authority to sign Federal Register
notices pertaining to announcements of
meetings and other committee
management activities, for both the
Centers for Disease Control and
Prevention and the Agency for Toxic
Substances and Disease Registry.
Dated: September 12, 2011.
Elaine L. Baker,
Director, Management Analysis and Services
Office, Centers for Disease Control and
Prevention.
[FR Doc. 2011–23767 Filed 9–15–11; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[Document Identifier: CMS–10398]
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;
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(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; Title of
Information Collection: Generic
Clearance for Medicaid and CHIP State
Plan, Waiver, and Program Submissions;
Use: CMS is requesting a generic PRA
clearance for a body of forms necessary
to conduct ongoing business with State
partners in the implementation of
Medicaid and the Children’s Health
Insurance Program (CHIP). Examples of
the types of forms to be produced in this
collection include State plan
amendment templates, waiver and
demonstration templates, and reporting
templates. The development of
streamlined submission forms is critical
for States to implement timely health
reform initiatives in Medicaid and CHIP
state plans, demonstrations, and
waivers, including legislative
requirements enacted by the Affordable
Care Act. The development of
streamlined submissions forms
enhances the collaboration and
partnership between States and CMS by
documenting CMS policy for States to
use as they are developing program
changes. Streamlined forms improve
efficiency of administration by creating
a common and user-friendly
understanding of the information
needed by CMS to quickly process
requests for State plan amendments,
waivers, and demonstration, as well as
ongoing reporting.; Form Number:
CMS–10398 (OMB #0938–NEW);
Frequency: Occasionally; Affected
Public: State, Local, or Tribal
Governments; Number of Respondents:
56; Total Annual Responses: 1120; Total
Annual Hours: 28,747. (For policy
questions regarding this collection
contact Candice Payne at 410–786–
4453. 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
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Federal Register / Vol. 76, No. 180 / Friday, September 16, 2011 / Notices
be received by the OMB desk officer at
the address below, no later than 5 p.m.
on October 17, 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: September 13, 2011.
Martique Jones,
Director, Regulations Development Group,
Division B, Office of Strategic Operations and
Regulatory Affairs.
[FR Doc. 2011–23807 Filed 9–15–11; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[Document Identifier: CMS–R–246 and
CMS–10147]
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: Revision of a currently
approved collection; Title of
Information Collection: Medicare
Advantage, Medicare Part D and
Medicare Fee For Service Consumer
Assessment of Healthcare Providers and
Systems Survey. Use: CMS has fielded
the MA Consumer Assessment of Health
Care Providers and Systems (CAHPS)
Survey annually since 1998, the
Medicare FFS CAHPS Survey annually
since 2000, and the MA DP and Stand
Alone PDP CAHPS survey annually
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since 2006. The Medicare CAHPS is a
national survey of health and
prescription drug plans conducted at
the contract level for MA, MA PD and
Stand Alone PDP plans and at the state
level for Medicare fee-for-service.
Medicare CAHPS provides data to
permit preparation of plan performance
measures to assist Medicare
beneficiaries in their selection of a
health plan, prescription drug plan or
both, and help policymakers and others
assist the Medicare program and
Medicare plans design and monitor
patient-centered quality improvement
initiatives. The 2009 Call letter for MA
and MA PD plans requires these plans
to contract with private vendors from a
list selected by CMS to conduct the
2011 Medicare CAHPS survey for their
plan at the contract level and provide
the collected data to CMS for analyses
and preparation of CAHPS measures for
use in consumer and plan reports and
for quality improvement purposes for
MA, MA PD, and Stand Alone PDP
plans. CMS will continue to collect the
Medicare FFS CAHPS data from surveys
at the state and some sub-state levels.
This revision to a currently approved
collection is to add questions focusing
on care coordination. Form Number:
CMS–R–246 (OCN: 0938–0732)
Frequency: Yearly; Affected Public:
Private Sector—Business or other Forprofits; Number of Respondents:
598,200; Number of Responses: 598,200;
Total Annual Hours: 216,555. (For
policy questions regarding this
collection, contact Sarah Gaillot at 410–
786–4637. For all other issues call (410)
786–1326.)
2. Type of Information Collection
Request: Revision of a currently
approved collection; Title of
Information Collection: Standardized
Pharmacy Notice: Your Prescription
Cannot be Filled (f/k/a Medicare
Prescription Drug Coverage and Your
Rights) Use: This is a request for
approval of changes to a currently
approved collection under 42 CFR
423.562(a)(3). This regulatory provision
has recently been modified to eliminate
the previously available option of
posting the standardized notice at the
pharmacy. Revised 423.562(a)(3) and an
associated regulatory provision at
§ 423.128(b)(7)(iii) require the pharmacy
to provide the Part D enrollee with a
printed copy of this standardized notice
if the prescription cannot be filled.
The purpose of this notice is to
provide enrollees with information
about how to contact their Part D plans
to request a coverage determination,
including a request for an exception to
the Part D plan’s formulary. The notice
reminds enrollees about certain rights
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and protections related to their
Medicare prescription drug benefits,
including the right to receive a written
explanation from the drug plan about
why a prescription drug is not covered.
A Part D plan sponsor’s network
pharmacies are in the best position to
notify enrollees about how to contact
their Part D plan if the prescription
cannot be filled.
As noted in a final rule published
April 15, 2011 (76 FR 21432), the option
of posting this notice at the pharmacy
has been eliminated. If a prescription
cannot be filled, the pharmacy must
provide the enrollee with a printed copy
of this notice. Form Number: CMS–
10147 (OCN: 0938–0975) Frequency:
Yearly; Affected Public: Private Sector—
Business or other For-profits; Number of
Respondents: 42,000; Number of
Responses: 37,087,402; Total Annual
Hours: 617,876. (For policy questions
regarding this collection, contact
Kathryn McCann Smith at 410–786–
7623. 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 October 17, 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: September 13, 2011.
Martique Jones,
Director, Regulations Development Group,
Division B, Office of Strategic Operations and
Regulatory Affairs.
[FR Doc. 2011–23801 Filed 9–15–11; 8:45 am]
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Agencies
[Federal Register Volume 76, Number 180 (Friday, September 16, 2011)]
[Notices]
[Pages 57744-57745]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2011-23807]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Medicare & Medicaid Services
[Document Identifier: CMS-10398]
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: New collection; Title of
Information Collection: Generic Clearance for Medicaid and CHIP State
Plan, Waiver, and Program Submissions; Use: CMS is requesting a generic
PRA clearance for a body of forms necessary to conduct ongoing business
with State partners in the implementation of Medicaid and the
Children's Health Insurance Program (CHIP). Examples of the types of
forms to be produced in this collection include State plan amendment
templates, waiver and demonstration templates, and reporting templates.
The development of streamlined submission forms is critical for States
to implement timely health reform initiatives in Medicaid and CHIP
state plans, demonstrations, and waivers, including legislative
requirements enacted by the Affordable Care Act. The development of
streamlined submissions forms enhances the collaboration and
partnership between States and CMS by documenting CMS policy for States
to use as they are developing program changes. Streamlined forms
improve efficiency of administration by creating a common and user-
friendly understanding of the information needed by CMS to quickly
process requests for State plan amendments, waivers, and demonstration,
as well as ongoing reporting.; Form Number: CMS-10398 (OMB
0938-NEW); Frequency: Occasionally; Affected Public: State,
Local, or Tribal Governments; Number of Respondents: 56; Total Annual
Responses: 1120; Total Annual Hours: 28,747. (For policy questions
regarding this collection contact Candice Payne at 410-786-4453. 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
[[Page 57745]]
be received by the OMB desk officer at the address below, no later than
5 p.m. on October 17, 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: September 13, 2011.
Martique Jones,
Director, Regulations Development Group, Division B, Office of
Strategic Operations and Regulatory Affairs.
[FR Doc. 2011-23807 Filed 9-15-11; 8:45 am]
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