Advisory Committee to the Director (ACD), Centers for Disease Control and Prevention (CDC)-Ethics Subcommittee (ES), 57744 [2011-23767]
Download as PDF
<![CDATA[
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
mstockstill on DSK4VPTVN1PROD with NOTICES
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]
BILLING CODE 4160–01–P
VerDate Mar<15>2010
16:26 Sep 15, 2011
Jkt 223001
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]
BILLING CODE 4163–18–P
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;
AGENCY:
PO 00000
Frm 00033
Fmt 4703
Sfmt 4703
(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
E:\FR\FM\16SEN1.SGM
16SEN1
]]>Agencies
[Federal Register Volume 76, Number 180 (Friday, September 16, 2011)]
[Notices]
[Page 57744]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2011-23767]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Disease Control and Prevention
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]
BILLING CODE 4163-18-P
