Proposed Information Collection Activity; Comment Request, 1954-1955 [2016-00595]
Download as PDF
<![CDATA[
1954
Federal Register / Vol. 81, No. 9 / Thursday, January 14, 2016 / Notices
Each PRC is housed within an
accredited school of public health or an
accredited school of medicine or
osteopathy with a preventive medicine
residency program. The PRCs conduct
outcomes-oriented, applied prevention
research on a broad range of topics
using a multi-disciplinary and
community-engaged approach. Each
PRC receives funding from the CDC to
establish its core infrastructure and
functions and support a core research
project. In addition to core research
projects, most PRCs are awarded
funding to complete special interest
projects (SIPs) and conduct other
research projects.
The DP14–001 program
announcement included language that
was used to develop and operationalize
a set of 25 PRC Program evaluation
indicators. The PRC Program logic
model identifies program inputs,
activities, outputs, and outcomes. The
list of indicators was revised to better
reflect program needs and capture PRCs’
center and research activities, outputs,
and outcomes.
The CDC is currently approved to
collect information from the PRCs
through a structured telephone
interview and a web-based survey
hosted by a third-party. The web-based
survey is designed to collect
information on the PRCs’ collaborations
with health departments; formal
training programs and other training
activities; and other-funded research
projects conducted separate from their
core projects or SIP research. Structured
telephone interviews with key PRC
informants allow PRC Program staff to
collect indicator data that do not lend
themselves to a survey-based
methodology and require a qualitative
approach.
CDC requests OMB approval to revise
the information collection plan as
follows:
(1) The content of the web-based survey
will be updated to more closely align with
revised evaluation indicators. In addition, the
web-based survey will be migrated from a
third party platform to a web-based data
collection system hosted on CDC servers.
Although the estimated burden per response
will increase, the revised data collection
system will be comprehensive and will
reduce the need for follow-up clarification by
PRC Program awardees.
(2) CDC will discontinue telephone
interviews and conduct key informant
interviews (KII) every other year to capture
qualitative information about PRC Network
formation and cohesion.
CDC will continue to use the
information reported by PRCs to
identify training and technical
assistance needs, respond to requests for
information from Congress and other
sources, monitor grantees’ compliance
with cooperative agreement
requirements, evaluate progress made in
achieving goals and objectives, and
describe the impact and effectiveness of
the PRC Program.
The CDC currently funds 26 PRCs.
Each PRC will annually report the
required information to the CDC. The
annualized estimated burden is
expected to increase. This increase
equates to an estimated weekly burden
of one hour per respondent and more
fully accounts for the burden of
preparing responses, as well as the
burden of reporting responses. Webbased data collection will occur on an
annual basis. The KIIs will take place in
2016 and 2018. This equates to two PRC
Network KIIs per PRC Program awardee
during the three year OMB approval
period. Responses are annualized in the
burden table below.
The proposed web-based data
collection system will allow data entry
during the entire year, which will
enable respondents to distribute burden
throughout each funding year. Response
burden is expected to decrease in
funding years 2 through 5, since the
web-based data collection system will
replicate a number of data elements
from year-to-year, and respondents will
only need to enter changes.
OMB approval is requested for three
years. CDC plans to implement revised
reporting requirements in March 2016.
PRC Program awardees are required to
participate in information collection.
There are no costs to respondents other
than their time. The total estimated
annualized burden hours are 1,299.
ESTIMATED ANNUALIZED BURDEN HOURS
Number of
respondents
Type of respondent
Form name
Prevention Research Center ..
Web-based Data Collection ...................................................
Key Informant Interview: PRCs Network ...............................
Leroy A. Richardson,
Chief, Information Collection Review Office,
Office of Scientific Integrity, Office of the
Associate Director for Science, Office of the
Director, Centers for Disease Control and
Prevention.
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Children and
Families
[OMB No. 0970–0410]
BILLING CODE 4163–18–P
mstockstill on DSK4VPTVN1PROD with NOTICES
[FR Doc. 2016–00563 Filed 1–13–16; 8:45 am]
Proposed Information Collection
Activity; Comment Request
Title: Tribal PREP Implementation
Plan.
Description: This request to collect
information for the Tribal PREP
Implementation Plan, is due by July 1,
VerDate Sep<11>2014
16:39 Jan 13, 2016
Jkt 238001
PO 00000
Frm 00018
Fmt 4703
Sfmt 4703
26
17
Number of
responses per
respondent
1
1
Average
burden per
response
(in hrs.)
48
3
2017. This plan will contain the
description of how the grantee intends
to structure, measure and evaluate the
implementation of the project.
Information contained in this
Implementation Plan will enable the
Program Office to provide the necessary
technical assistance to help ensure that
grantees are structuring Tribal PREP
projects within the framework of PREP
design guidance, including mandated
adult preparation subjects, Positive
Youth Development and evidence-based
programming.
Respondents:
E:\FR\FM\14JAN1.SGM
14JAN1
1955
Federal Register / Vol. 81, No. 9 / Thursday, January 14, 2016 / Notices
ANNUAL BURDEN ESTIMATES
Instrument
Number of
respondents
Number of
responses per
respondent
Average
burden hours
per response
Total burden
hours
Tribal PREP Plan .............................................................................................
10
1
40
400
Estimated Total Annual Burden
Hours: 400.
In compliance with the requirements
of Section 3506(c)(2)(A) of the
Paperwork Reduction Act of 1995, the
Administration for Children and
Families is soliciting public comment
on the specific aspects of the
information collection described above.
Copies of the proposed collection of
information can be obtained and
comments may be forwarded by writing
to the Administration for Children and
Families, Office of Administration,
Office of Information Services, 370
L’Enfant Promenade SW., Washington,
DC 20447, Attn: ACF Reports Clearance
Officer. Email address: infocollection@
acf.hhs.gov. All requests should be
identified by the title of the information
collection.
The Department specifically requests
comments on: (a) whether the proposed
collection of information is necessary
for the proper performance of the
functions of the agency, including
whether the information shall have
practical utility; (b) the accuracy of the
agency’s estimate of the burden of the
proposed collection of information; (c)
the quality, utility, and clarity of the
information to be collected; and (d)
ways to minimize the burden of the
collection of information on
respondents, including through the use
of automated collection techniques or
other forms of information technology.
Consideration will be given to
comments and suggestions submitted
within 60 days of this publication.
Robert Sargis,
Reports Clearance Officer.
[FR Doc. 2016–00595 Filed 1–13–16; 8:45 am]
BILLING CODE 4184–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
mstockstill on DSK4VPTVN1PROD with NOTICES
[Docket No. FDA–2015–N–4809]
Patient and Medical Professional
Perspectives on the Return of Genetic
Test Results and Interpretations;
Public Workshop; Request for
Comments
AGENCY:
Food and Drug Administration,
HHS.
VerDate Sep<11>2014
18:58 Jan 13, 2016
Jkt 238001
Notice of public workshop;
request for comments.
ACTION:
The Food and Drug
Administration (FDA) is announcing the
following public workshop entitled
‘‘Patient and Medical Professional
Perspectives on the Return of Genetic
Test Results.’’ The purpose of this
public workshop is to understand
patient and provider perspectives on
receiving potentially medically relevant
genetic test results. The topic(s) to be
discussed will focus on better defining
the specific information patients and
providers prefer to receive, with an
emphasis on the type(s) and amount of
evidence available to interpret the
results for medical purposes, how those
results should be returned, and what
information is needed to understand the
results in the event that they could
effectively aid in medical decision
making.
DATES: The public workshop will be
held on March 2, 2016, from 8 a.m. to
4 p.m. Submit either electronic or
written comments on the public
workshop by March 31, 2016.
ADDRESSES: The public workshop will
be held at FDA’s White Oak Campus,
10903 New Hampshire Ave., Bldg. 31
Conference Center, the Great Room (Rm.
1503), Silver Spring, MD 20993.
Entrance for the public meeting
participants (non-FDA employees) is
through Building 1, where routine
security check procedures will be
performed. For parking and security
information, please refer to https://www.
fda.gov/AboutFDA/WorkingatFDA/
BuildingsandFacilities/WhiteOak
CampusInformation/ucm241740.htm.
You may submit comments as
follows:
SUMMARY:
Electronic Submissions
Submit electronic comments in the
following way:
• Federal eRulemaking Portal: https://
www.regulations.gov. Follow the
instructions for submitting comments.
Comments submitted electronically,
including attachments, to https://
www.regulations.gov will be posted to
the docket unchanged. Because your
comment will be made public, you are
solely responsible for ensuring that your
comment does not include any
confidential information that you or a
PO 00000
Frm 00019
Fmt 4703
Sfmt 4703
third party may not wish to be posted,
such as medical information, your or
anyone else’s Social Security number, or
confidential business information, such
as a manufacturing process. Please note
that if you include your name, contact
information, or other information that
identifies you in the body of your
comments, that information will be
posted on https://www.regulations.gov.
• If you want to submit a comment
with confidential information that you
do not wish to be made available to the
public, submit the comment as a
written/paper submission and in the
manner detailed (see ‘‘Written/Paper
Submissions’’ and ‘‘Instructions’’).
Written/Paper Submissions
Submit written/paper submissions as
follows:
• Mail/Hand delivery/Courier (for
written/paper submissions): Division of
Dockets Management (HFA–305), Food
and Drug Administration, 5630 Fishers
Lane, Rm. 1061, Rockville, MD 20852.
• For written/paper comments
submitted to the Division of Dockets
Management, FDA will post your
comment, as well as any attachments,
except for information submitted,
marked and identified, as confidential,
if submitted as detailed in
‘‘Instructions.’’
Instructions: All submissions received
must include the Docket No. FDA–
2015–N–4809 for ‘‘Patient and Medical
Professional Perspectives on the Return
of Genetic Test Results; Public
Workshop; Request for Comments.’’
Received comments will be placed in
the docket and, except for those
submitted as ‘‘Confidential
Submissions,’’ publicly viewable at
https://www.regulations.gov or at the
Division of Dockets Management
between 9 a.m. and 4 p.m., Monday
through Friday.
• Confidential Submissions—To
submit a comment with confidential
information that you do not wish to be
made publicly available, submit your
comments only as a written/paper
submission. You should submit two
copies total. One copy will include the
information you claim to be confidential
with a heading or cover note that states
‘‘THIS DOCUMENT CONTAINS
CONFIDENTIAL INFORMATION’’. The
Agency will review this copy, including
E:\FR\FM\14JAN1.SGM
14JAN1
]]>Agencies
[Federal Register Volume 81, Number 9 (Thursday, January 14, 2016)]
[Notices]
[Pages 1954-1955]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2016-00595]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Administration for Children and Families
[OMB No. 0970-0410]
Proposed Information Collection Activity; Comment Request
Title: Tribal PREP Implementation Plan.
Description: This request to collect information for the Tribal
PREP Implementation Plan, is due by July 1, 2017. This plan will
contain the description of how the grantee intends to structure,
measure and evaluate the implementation of the project. Information
contained in this Implementation Plan will enable the Program Office to
provide the necessary technical assistance to help ensure that grantees
are structuring Tribal PREP projects within the framework of PREP
design guidance, including mandated adult preparation subjects,
Positive Youth Development and evidence-based programming.
Respondents:
[[Page 1955]]
Annual Burden Estimates
----------------------------------------------------------------------------------------------------------------
Number of Average burden
Instrument Number of responses per hours per Total burden
respondents respondent response hours
----------------------------------------------------------------------------------------------------------------
Tribal PREP Plan............................ 10 1 40 400
----------------------------------------------------------------------------------------------------------------
Estimated Total Annual Burden Hours: 400.
In compliance with the requirements of Section 3506(c)(2)(A) of the
Paperwork Reduction Act of 1995, the Administration for Children and
Families is soliciting public comment on the specific aspects of the
information collection described above. Copies of the proposed
collection of information can be obtained and comments may be forwarded
by writing to the Administration for Children and Families, Office of
Administration, Office of Information Services, 370 L'Enfant Promenade
SW., Washington, DC 20447, Attn: ACF Reports Clearance Officer. Email
address: infocollection@acf.hhs.gov. All requests should be identified
by the title of the information collection.
The Department specifically requests comments on: (a) whether the
proposed collection of information is necessary for the proper
performance of the functions of the agency, including whether the
information shall have practical utility; (b) the accuracy of the
agency's estimate of the burden of the proposed collection of
information; (c) the quality, utility, and clarity of the information
to be collected; and (d) ways to minimize the burden of the collection
of information on respondents, including through the use of automated
collection techniques or other forms of information technology.
Consideration will be given to comments and suggestions submitted
within 60 days of this publication.
Robert Sargis,
Reports Clearance Officer.
[FR Doc. 2016-00595 Filed 1-13-16; 8:45 am]
BILLING CODE 4184-01-P
