Proposed Collection; 60-Day Comment Request; Web-based Media Literacy Parent Training for Substance Use Prevention in Rural Locations, 18612-18613 [2013-07038]
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18612
Federal Register / Vol. 78, No. 59 / Wednesday, March 27, 2013 / Notices
requests are to be sent to the Division
of Freedom of Information (ELEM–
1029), Food and Drug Administration,
12420 Parklawn Dr., Element Bldg.,
Rockville, MD 20857. A link to the
transcripts will also be available
approximately 45 days after the public
workshop on the Internet at https://
www.fda.gov/MedicalDevices/
NewsEvents/WorkshopsConferences/
default.htm. (Select this public
workshop from the posted events list).
SUPPLEMENTARY INFORMATION:
mstockstill on DSK4VPTVN1PROD with NOTICES
I. Background
There is increased utilization of color
in several areas of medical imaging and
a wider range of availability of a variety
of hardware and software platforms that
rely on medical and non-medical
devices to implement medical imaging
product solutions for color imagery.
This new reality has brought up issues
related to the interoperability of devices
and to the framework of accurately
dealing with color data in medical
imaging products. This workshop brings
together key stakeholders to clearly
identify areas of need, investigate
solutions and propose best-practice
approaches. The recommendations of
the summit might include the creation
of a technical special interest group
either as part of the ICC or in some other
forum and the establishment of bestpractice guidelines for industry. The
summit will address emerging
utilization of color in medical imaging
in areas including clinical photography,
ophthalmic photography, digital
microscopy, digital histopathology,
endoscopy, laparoscopy, telemedicine,
handheld mobile displays, display
devices, color measurement, and
standards and professional group
recommendations from organizations
such as the Digital Imaging and
Communications in Medicine, ICC,
International Commission on
Illumination, International
Electrotechnical Commission, and
American Association of Physicists in
Medicine.
I. Topics
There is increasing use of color in
medical imaging but so far there is no
clear definition of a technical
framework for color management across
the imaging chain from acquisition, preand post-processing, to storage, transfer
and display. Due to the increasing use
of color images and the need for
integrated electronic health records, this
issue is of current relevance for device
manufacturers, users, and regulators. In
addition, topics might include color
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methods for handheld display devices,
system approaches for color
consistency, and inter-vendor
interoperability.
Scheduled session topics include: (1)
General landscape of color use in
medical imaging, (2) whole-slide
imagers and digital microscopy/
histopathology, (3) endoscopy and
laparoscopy, (4) other medical imaging
modalities, (5) standards and
professional organization
recommendations, (6) color in
telemedicine, and (7) color in mobile
displays.
Dated: March 22, 2013.
Leslie Kux,
Assistant Commissioner for Policy.
[FR Doc. 2013–07031 Filed 3–26–13; 8:45 am]
BILLING CODE 4160–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
Proposed Collection; 60-Day Comment
Request; Web-based Media Literacy
Parent Training for Substance Use
Prevention in Rural Locations
SUMMARY: In compliance with the
requirement 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 Institute on Drug Abuse
(NIDA), 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 on 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)
Ways to enhance the quality, utility, and
clarity of the information to be
collected; and (4) Ways to 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 and For Further
Information: To obtain a copy of the
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Fmt 4703
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data collection plans and instruments,
contact Dr. Augie Diana, Health
Scientist Administrator, Prevention
Research Branch, Division of
Epidemiology, Services, and Prevention
Research, NIDA, NIH, 6001 Executive
Boulevard, Room 5163, Bethesda, MD
20892, or call non-toll-free number (301)
443–1942 or Email your request,
including your address to:
dianaa@nida.nih.gov. Formal requests
for additional plans and instruments
must be requested in writing.
Comments Due Date: 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: Web-based
Media Literacy Parent Training for
Substance Use Prevention in Rural
Locations, 0925-New, National Institute
on Drug Abuse (NIDA), National
Institutes of Health (NIH).
Need and Use of Information
Collection: This study will develop a
web-based media literacy substance use
prevention intervention for use with
parents and their elementary school
children (approximately ages 7–12), and
will evaluate the program in a
randomized controlled trial to establish
program efficacy in six rural
communities in North Carolina and
Texas. The primary objectives of the
study are to assess the efficacy of a
media literacy education program that is
specifically designed to overcome
barriers to prevention efforts in rural
communities, and to provide the
scientific basis for establishing the
program, Media Detective Family, as an
evidence-based substance use
prevention curriculum. The information
will provide valuable information
concerning: (1) The appropriateness of
using technology for substance use
prevention programming (i.e., internet,
Smartphone, or tablet-based
applications) to reach rural families
with elementary school-aged children;
(2) improvements in parents’ and
children’s critical thinking skills
associated with intervention exposure;
(3) improvements in parent-child
communication about substances and
the media associated with intervention
exposure; and (4) reductions in
children’s behavioral intentions to use
substances associated with intervention
exposure.
OMB approval is requested for two
years. There are no costs to respondents
other than their time. The total
estimated annualized burden hours are
1067.
E:\FR\FM\27MRN1.SGM
27MRN1
18613
Federal Register / Vol. 78, No. 59 / Wednesday, March 27, 2013 / Notices
ESTIMATED ANNUALIZED BURDEN HOURS
Number of
respondents
Type of respondents
Adults
Pretest ......................................................................................................
Posttest .....................................................................................................
Follow-up ..................................................................................................
Usage Log ................................................................................................
Children
Pretest ......................................................................................................
Posttest .....................................................................................................
Follow-up ..................................................................................................
Dated: March 20, 2013.
Helio Chaves,
Deputy Director Office of Management, NIDA,
NIH.
[FR Doc. 2013–07038 Filed 3–26–13; 8:45 am]
BILLING CODE 4140–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
Notice of the Implementation of the
National Institutes of Health (NIH)
Electronic Vendor Invoice Program
(eVIP)
SUMMARY: The purpose of this notice is
to announce the future implementation
of the Electronic Vendor Invoice
Program (eVIP) at the National Institutes
of Health (NIH) and the planned
modification of NIH awards to require
vendors to use the eVIP in future
contracts.
mstockstill on DSK4VPTVN1PROD with NOTICES
FOR FURTHER INFORMATION CONTACT:
Darlene Walls, The Division of
Acquisition Policy and Evaluation, The
National Institutes of Health, 6100
Executive Blvd., Rockville, Maryland
20852 or PPMB@mail.nih.gov.
SUPPLEMENTARY INFORMATION: Electronic
invoicing will enhance compliance with
laws and regulations that govern the
accuracy, timeliness, and costeffectiveness of the Federal
Government’s payment process.
Executive Order 13576, Delivering an
Efficient, Effective, and Accountable
Government, issued June 13, 2011,
requires Federal Government agencies
to become more effective and efficient,
cut waste, and streamline Government
operations. The Federal Acquisition
Regulation (FAR) subpart 32.9
prescribes policies, procedures, and
clauses for implementing prompt
payment regulations. Electronic invoice
submission through eVIP will reduce
inefficiencies related to paper-based
invoicing, reduce interest payments
caused by late payments of invoices,
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Frm 00055
Fmt 4703
Average time
per response
Annual hour
burden
200
........................
........................
........................
1
1
1
2
1
45/60
45/60
10/60
200.00
150.00
150.00
67.00
200
........................
........................
1
1
1
1
45/60
45/60
200.00
150.00
150.00
and ultimately foster the prompt
payment of invoices to vendors.
Public Law 111–204, Improper
Payments Elimination and Recovery Act
of 2010, requires Federal Government
agencies to periodically review all
programs and identify the programs and
activities that may be susceptible to
significant improper payments. Section
2(h)(4) of Public Law 111–204 requires
the head of the agency to conduct a
financial management improvement
program, consistent with the rules
prescribed by the Director of the Office
of Management and Budget.
The first priority of the program must
address problems that contribute
directly to the agency improper
payments. The eVIP solution allows for
vendor invoices to be matched to the
award document electronically, thereby
minimizing processing errors associated
with invoice mailing, invoice scanning,
or invoice entry and enhances the
ability to make proper invoice
payments. Ultimately, the eVIP solution
is expected to result in a decrease in
interest payments, an increase in data
accuracy, and provide an enhanced
ability to make proper invoice
payments.
The eVIP will be implemented in
three phases, Phase I Pilot, Phase II
Pilot, and Roll-Out:
Phase I Pilot: Phase I was initiated in
October 2009. Four pilot vendors were
provisioned in the electronic system to
test the functionality for viewing
invoices, and later, submitting invoices
for payment. Lessons learned were
gathered from the feedback received and
areas for improvement were identified.
Phase II Pilot: Enhancements in
processes are being made to the
electronic payment system based on the
lessons learned during Phase I. Six
additional vendors will be added and
both Phase I and Phase II vendors will
be provisioned using a authentication
process different from that available in
Phase I, and will be provided access to
view invoices and submit invoices for
payment.
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Frequency of
response
Sfmt 4703
Roll-Out: Phase II will be initiated in
March 2013. The results of the Phase II
effort will be assessed prior to formal
implementation of the eVIP initiative. It
is anticipated that implementation will
occur through the use of a phased
approach, beginning in October 2013.
Dated: March 9, 2013.
Lawrence A. Tabak,
Deputy Director, National Institutes of Health.
[FR Doc. 2013–07037 Filed 3–26–13; 8:45 am]
BILLING CODE 4140–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
National Institutes of Health
National Institute of Diabetes and
Digestive and Kidney Diseases Notice
of Closed Meeting
Pursuant to section 10(d) of the
Federal Advisory Committee Act, as
amended (5 U.S.C. App.), notice is
hereby given of the following meeting.
The meeting will be closed to the
public in accordance with the
provisions set forth in sections
552b(c)(4) and 552b(c)(6), Title 5 U.S.C.,
as amended. The grant applications and
the discussions could disclose
confidential trade secrets or commercial
property such as patentable material,
and personal information concerning
individuals associated with the grant
applications, the disclosure of which
would constitute a clearly unwarranted
invasion of personal privacy.
Name of Committee: National Institute of
Diabetes and Digestive and Kidney Diseases
Special Emphasis Panel; Developmental
Centers in Benign Urology (P20s, RFA–DK–
12–022)
Date: May 17, 2013.
Time: 8:30 a.m. to 5:00 p.m.
Agenda: To review and evaluate grant
applications.
Place: Hyatt Regency Bethesda, One
Bethesda Metro Center, 7400 Wisconsin
Avenue, Bethesda, MD 20814.
Contact Person: Najma Begum, Ph.D.,
Scientific Review Officer, Review Branch,
DEA, NIDDK, National Institutes Of Health,
E:\FR\FM\27MRN1.SGM
27MRN1
]]>Agencies
[Federal Register Volume 78, Number 59 (Wednesday, March 27, 2013)]
[Notices]
[Pages 18612-18613]
From the Federal Register Online via the Government Printing Office [www.gpo.gov]
[FR Doc No: 2013-07038]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
National Institutes of Health
Proposed Collection; 60-Day Comment Request; Web-based Media
Literacy Parent Training for Substance Use Prevention in Rural
Locations
SUMMARY: In compliance with the requirement 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 Institute on Drug
Abuse (NIDA), 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 on 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) Ways to enhance the quality, utility, and clarity of the
information to be collected; and (4) Ways to 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 and For Further Information: To obtain a copy of
the data collection plans and instruments, contact Dr. Augie Diana,
Health Scientist Administrator, Prevention Research Branch, Division of
Epidemiology, Services, and Prevention Research, NIDA, NIH, 6001
Executive Boulevard, Room 5163, Bethesda, MD 20892, or call non-toll-
free number (301) 443-1942 or Email your request, including your
address to: dianaa@nida.nih.gov. Formal requests for additional plans
and instruments must be requested in writing.
Comments Due Date: 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: Web-based Media Literacy Parent Training for
Substance Use Prevention in Rural Locations, 0925-New, National
Institute on Drug Abuse (NIDA), National Institutes of Health (NIH).
Need and Use of Information Collection: This study will develop a
web-based media literacy substance use prevention intervention for use
with parents and their elementary school children (approximately ages
7-12), and will evaluate the program in a randomized controlled trial
to establish program efficacy in six rural communities in North
Carolina and Texas. The primary objectives of the study are to assess
the efficacy of a media literacy education program that is specifically
designed to overcome barriers to prevention efforts in rural
communities, and to provide the scientific basis for establishing the
program, Media Detective Family, as an evidence-based substance use
prevention curriculum. The information will provide valuable
information concerning: (1) The appropriateness of using technology for
substance use prevention programming (i.e., internet, Smartphone, or
tablet-based applications) to reach rural families with elementary
school-aged children; (2) improvements in parents' and children's
critical thinking skills associated with intervention exposure; (3)
improvements in parent-child communication about substances and the
media associated with intervention exposure; and (4) reductions in
children's behavioral intentions to use substances associated with
intervention exposure.
OMB approval is requested for two years. There are no costs to
respondents other than their time. The total estimated annualized
burden hours are 1067.
[[Page 18613]]
Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
Number of Frequency of Average time Annual hour
Type of respondents respondents response per response burden
----------------------------------------------------------------------------------------------------------------
Adults
Pretest..................................... 200 1 1 200.00
Posttest.................................... .............. 1 45/60 150.00
Follow-up................................... .............. 1 45/60 150.00
Usage Log................................... .............. 2 10/60 67.00
Children
Pretest..................................... 200 1 1 200.00
Posttest.................................... .............. 1 45/60 150.00
Follow-up................................... .............. 1 45/60 150.00
----------------------------------------------------------------------------------------------------------------
Dated: March 20, 2013.
Helio Chaves,
Deputy Director Office of Management, NIDA, NIH.
[FR Doc. 2013-07038 Filed 3-26-13; 8:45 am]
BILLING CODE 4140-01-P
