Proposed Collection; Comment Request (60-Day FRN); A Generic Submission for Formative Research, Pretesting, and Customer Satisfaction of NCI's Communication and Education Resources (NCI), 105-106 [2012-31503]
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Federal Register / Vol. 78, No. 1 / Wednesday, January 2, 2013 / Notices
105
TABLE 1—Continued
Committee name
Tentative date(s) of meeting(s)
CENTER FOR DEVICES AND RADIOLOGICAL HEALTH
Medical Devices Advisory Committee (Comprised of 18 Panels)
Anesthesiology and Respiratory Therapy Devices Panel ........................
Circulatory System Devices Panel ...........................................................
Clinical Chemistry and Clinical Toxicology Devices Panel ......................
Dental Products Panel ..............................................................................
Ear, Nose, and Throat Devices Panel .....................................................
Gastroenterology-Urology Devices Panel ................................................
General and Plastic Surgery Devices Panel ............................................
General Hospital and Personal Use Devices Panel ................................
Hematology and Pathology Devices Panel ..............................................
Immunology Devices Panel ......................................................................
Medical Devices Dispute Resolution Panel .............................................
Microbiology Devices Panel .....................................................................
Molecular and Clinical Genetics Panel ....................................................
Neurological Devices Panel .....................................................................
Obstetrics and Gynecology Devices Panel ..............................................
Ophthalmic Devices Panel .......................................................................
Orthopaedic and Rehabilitation Devices Panel ........................................
Radiological Devices Panel ......................................................................
Device Good Manufacturing Practice Advisory Committee .....................
National Mammography Quality Assurance Advisory Committee ...........
Technical Electronic Product Radiation Safety Standards Committee ....
Date(s), if needed, to be determined.
May 17, May 24, June 27, September 27, November 22.
April 25.
Date(s), if needed, to be determined.
July 12.
April 24, May 16.
June 13.
June 28, August 30.
Date(s), if needed, to be determined.
Date(s), if needed, to be determined.
Date(s), if needed, to be determined.
June 14.
September 13.
February 22.
September 20.
June 14, August 23.
April 5, September 26.
September 12.
April 11.
October 25.
Date(s), if needed, to be determined.
CENTER FOR FOOD SAFETY AND APPLIED NUTRITION
Food Advisory Committee ........................................................................
July 15–16, August 29–30, September 23–24.
CENTER FOR TOBACCO PRODUCTS
Tobacco Products Scientific Advisory Committee ...................................
Feb 11–12, April 30–May 1.
CENTER FOR VETERINARY MEDICINE
Veterinary Medicine Advisory Committee ................................................
Date(s), if needed, to be determined.
NATIONAL CENTER FOR TOXICOLOGICAL RESEARCH (NCTR)
Science Advisory Board to NCTR ............................................................
Dated: December 26, 2012.
Leslie Kux,
Assistant Commissioner for Policy.
[FR Doc. 2012–31475 Filed 12–31–12; 8:45 am]
BILLING CODE 4160–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES\
National Institutes of Health
Proposed Collection; Comment
Request (60-Day FRN); A Generic
Submission for Formative Research,
Pretesting, and Customer Satisfaction
of NCI’s Communication and
Education Resources (NCI)
Under the provisions of
Section 3506(c)(2)(A) of the Paperwork
Reduction Act of 1995, for opportunity
for public comment on proposed data
collection projects, the National
Institutes of Health (NIH) will publish
periodic summaries of proposed
tkelley on DSK3SPTVN1PROD with
SUMMARY:
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December 10–11.
projects to be submitted to the Office of
Management and Budget (OMB) for
review and approval.
Written comments and/or suggestions
from the public and affected agencies
are invited to address one or more of the
following points: (1) Whether the
proposed collection of information is
necessary for the proper performance of
the function of the agency, including
whether the information will have
practical utility; (2) The accuracy of the
agency’s estimate of the burden of the
proposed collection of information,
including the validity of the
methodology and assumptions used; (3)
The quality, utility, and clarity of the
information to be collected; and (4)
Minimize the burden of the collection of
information on those who are to
respond, including the use of
appropriate automated, electronic,
mechanical, or other technological
collection techniques or other forms of
information technology.
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To submit comments in writing,
request more information on the
proposed project, or to obtain a copy of
the data collection plans and
instruments, contact: Nina Goodman,
Public Health Advisor, Office of
Communications and Education (OCE),
NCI, NIH, 6116 Executive Blvd., Suite
400, Rockville, MD 20892, call non-tollfree number (301) 435–7789 or email
your request, including your address to:
goodmann@mail.nih.gov.
Comments regarding this information
collection are best assured of having
their full effect if received within 60
days of the date of this publication.
Proposed Collection: A Generic
Submission For Formative Research,
Pretesting, and Customer Satisfaction of
NCI’s Communication and Education
Resources, 0925–0046, Expiration Date
2/28/2013—EXTENSION—National
Cancer Institute, National Institutes of
Health (NIH).
Need and Use of Information
Collection: In order to carry out NCI’s
E:\FR\FM\02JAN1.SGM
02JAN1
106
Federal Register / Vol. 78, No. 1 / Wednesday, January 2, 2013 / Notices
legislative mandate to educate and
disseminate information about cancer
prevention, detection, diagnosis, and
treatment to a wide variety of audiences
and organizations, it is beneficial for
NCI through its Office of
Communications and Education (OCE),
to pretest NCI communications
strategies, concepts, and messages while
they are under development. This
pretesting, or formative evaluation,
helps ensure that the messages,
communication materials, and
information services created by NCI
have the greatest capacity of being
received, understood, and accepted by
their target audiences. Since NCI’s OCE
also is responsible for the design,
implementation, and evaluation of
education programs over the entire
cancer continuum, and management of
NCI initiatives that address specific
challenges in cancer research and
treatment, it is also necessary to ensure
that customers are satisfied with
programs. This customer satisfaction
research helps ensure the relevance,
utility, and appropriateness of the many
educational programs and products that
OCE and NCI produce. OCE will use a
variety of qualitative (focus groups,
interviews) and quantitative (paper,
phone, in-person, and web surveys)
methodologies to conduct this formative
and customer satisfaction research,
allowing NCI to: (1) Understand
characteristics (attitudes, beliefs, and
behaviors) of the intended target
audience and use this information in the
development of effective
communication tools and strategies; (2)
use a feedback loop to help refine,
revise, and enhance messages, materials,
products, and programs—ensuring that
they have the greatest relevance, utility,
appropriateness, and impact for/to
target audiences; and (3) expend limited
program resource dollars wisely and
effectively. The participants may
include, but are not limited to, cancer
patients, their families, the general
public, health providers, the media,
voluntary groups, scientific and medical
organizations (affected public could
include individuals or households;
businesses or other for profit; not-forprofit institutions; and Federal
Government; State, Local, or Tribal
Government).
OMB approval is requested for 3
years. There are no costs to respondents
other than their time. The total
estimated annualized burden hours are
6,600.
ESTIMATED ANNUALIZED BURDEN HOURS
Frequency of
response per
respondent
Number of
respondents
Category of respondents
Time per
response
(in hours)
Burden hours
Individuals, Households, Local, State, and Federal Governments, and Private Sector ...................................................................................................
33,000
1
12
6,600
Totals ........................................................................................................
33,000
........................
........................
6,600
Dated: December 20, 2012.
Vivian Horovitch-Kelley,
NCI Project Clearance Liaison, NCI, NIH.
[FR Doc. 2012–31503 Filed 12–31–12; 8:45 am]
BILLING CODE 4101–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
tkelley on DSK3SPTVN1PROD with
National Institute of Neurological
Disorders and Stroke, Interagency Pain
Research Coordinating Committee;
Call for Committee Membership
Nominations
The Department of Health and Human
Services (Department) has created the
Interagency Pain Research Coordinating
Committee and is seeking nominations
for this committee. As specified in
Public Law 111–148 (‘‘Patient
Protection and Affordable Care Act’’)
the Committee will: (a) Develop a
summary of advances in pain care
research supported or conducted by the
Federal agencies relevant to the
diagnosis, prevention, and treatment of
pain and diseases and disorders
associated with pain; (b) identify critical
gaps in basic and clinical research on
the symptoms and causes of pain; (c)
make recommendations to ensure that
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the activities of the National Institutes
of Health and other Federal agencies are
free of unnecessary duplication of effort;
(d) make recommendations on how best
to disseminate information on pain care;
and (e) make recommendations on how
to expand partnerships between public
entities and private entities to expand
collaborative, cross-cutting research.
Membership on the committee will
include six (6) non-Federal members
from among scientists, physicians, and
other health professionals and six (6)
non-Federal members of the general
public who are representatives of
leading research, advocacy, and service
organizations for individuals with painrelated conditions. Members will serve
overlapping three year terms. It is
anticipated that the committee will meet
at least once a year.
The Department strives to ensure that
the membership of HHS Federal
advisory committees is fairly balanced
in terms of points of view represented
and the committee’s function. Every
effort is made to ensure that the views
of women, all ethnic and racial groups,
and people with disabilities are
represented on HHS Federal advisory
committees and, therefore, the
Department encourages nominations of
qualified candidates from these groups.
The Department also encourages
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geographic diversity in the composition
of the Committee. Appointment to this
Committee shall be made without
discrimination on the basis of age, race,
ethnicity, gender, sexual orientation,
disability, and cultural, religious, or
socioeconomic status.
The Department is soliciting
nominations for two non-federal
members from among scientists,
physicians, and other health
professionals and for two non-federal
members of the general public who are
representatives of leading research,
advocacy, and service organizations for
people with pain-related conditions.
These candidates will be considered to
fill positions opened through
completion of member terms.
Nominations are due by COB, January
25, 2013, and should be sent to Linda
Porter, Ph.D., NINDS/NIH, 31 Center
Drive, Room 8A03, Bethesda, MD
20892, porterl@ninds.nih.gov by either
USPS mail or email. Nominations
should include contact information, and
a current curriculum vitae or resume.
Dated: November 18, 2012.
Linda L. Porter,
Health Science Policy Advisor for Pain,
National Institute of Neurological Disorders
and Stroke, National Institutes of Health.
[FR Doc. 2012–31508 Filed 12–31–12; 8:45 am]
BILLING CODE 4140–01–P
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02JAN1
Agencies
- National Institutes of Health
- DEPARTMENT OF HEALTH AND HUMAN SERVICES\
[Federal Register Volume 78, Number 1 (Wednesday, January 2, 2013)]
[Notices]
[Pages 105-106]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2012-31503]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES\
National Institutes of Health
Proposed Collection; Comment Request (60-Day FRN); A Generic
Submission for Formative Research, Pretesting, and Customer
Satisfaction of NCI's Communication and Education Resources (NCI)
SUMMARY: Under the provisions of Section 3506(c)(2)(A) of the Paperwork
Reduction Act of 1995, for opportunity for public comment on proposed
data collection projects, the National Institutes of Health (NIH) will
publish periodic summaries of proposed projects to be submitted to the
Office of Management and Budget (OMB) for review and approval.
Written comments and/or suggestions from the public and affected
agencies are invited to address one or more of the following points:
(1) Whether the proposed collection of information is necessary for the
proper performance of the function of the agency, including whether the
information will have practical utility; (2) The accuracy of the
agency's estimate of the burden of the proposed collection of
information, including the validity of the methodology and assumptions
used; (3) The quality, utility, and clarity of the information to be
collected; and (4) Minimize the burden of the collection of information
on those who are to respond, including the use of appropriate
automated, electronic, mechanical, or other technological collection
techniques or other forms of information technology.
To submit comments in writing, request more information on the
proposed project, or to obtain a copy of the data collection plans and
instruments, contact: Nina Goodman, Public Health Advisor, Office of
Communications and Education (OCE), NCI, NIH, 6116 Executive Blvd.,
Suite 400, Rockville, MD 20892, call non-toll-free number (301) 435-
7789 or email your request, including your address to:
goodmann@mail.nih.gov.
Comments regarding this information collection are best assured of
having their full effect if received within 60 days of the date of this
publication.
Proposed Collection: A Generic Submission For Formative Research,
Pretesting, and Customer Satisfaction of NCI's Communication and
Education Resources, 0925-0046, Expiration Date 2/28/2013--EXTENSION--
National Cancer Institute, National Institutes of Health (NIH).
Need and Use of Information Collection: In order to carry out NCI's
[[Page 106]]
legislative mandate to educate and disseminate information about cancer
prevention, detection, diagnosis, and treatment to a wide variety of
audiences and organizations, it is beneficial for NCI through its
Office of Communications and Education (OCE), to pretest NCI
communications strategies, concepts, and messages while they are under
development. This pretesting, or formative evaluation, helps ensure
that the messages, communication materials, and information services
created by NCI have the greatest capacity of being received,
understood, and accepted by their target audiences. Since NCI's OCE
also is responsible for the design, implementation, and evaluation of
education programs over the entire cancer continuum, and management of
NCI initiatives that address specific challenges in cancer research and
treatment, it is also necessary to ensure that customers are satisfied
with programs. This customer satisfaction research helps ensure the
relevance, utility, and appropriateness of the many educational
programs and products that OCE and NCI produce. OCE will use a variety
of qualitative (focus groups, interviews) and quantitative (paper,
phone, in-person, and web surveys) methodologies to conduct this
formative and customer satisfaction research, allowing NCI to: (1)
Understand characteristics (attitudes, beliefs, and behaviors) of the
intended target audience and use this information in the development of
effective communication tools and strategies; (2) use a feedback loop
to help refine, revise, and enhance messages, materials, products, and
programs--ensuring that they have the greatest relevance, utility,
appropriateness, and impact for/to target audiences; and (3) expend
limited program resource dollars wisely and effectively. The
participants may include, but are not limited to, cancer patients,
their families, the general public, health providers, the media,
voluntary groups, scientific and medical organizations (affected public
could include individuals or households; businesses or other for
profit; not-for-profit institutions; and Federal Government; State,
Local, or Tribal Government).
OMB approval is requested for 3 years. There are no costs to
respondents other than their time. The total estimated annualized
burden hours are 6,600.
Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Frequency of Time per
Category of respondents Number of response per response (in Burden hours
respondents respondent hours)
----------------------------------------------------------------------------------------------------------------
Individuals, Households, Local, State, and 33,000 1 12 6,600
Federal Governments, and Private Sector........
---------------------------------------------------------------
Totals...................................... 33,000 .............. .............. 6,600
----------------------------------------------------------------------------------------------------------------
Dated: December 20, 2012.
Vivian Horovitch-Kelley,
NCI Project Clearance Liaison, NCI, NIH.
[FR Doc. 2012-31503 Filed 12-31-12; 8:45 am]
BILLING CODE 4101-01-P