81 FR 1954 - Proposed Information Collection Activity; Comment Request
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Administration for Children and Families Federal Register Volume 81, Issue 9 (January 14, 2016)
Administration for Children and Families
Federal Register Volume 81, Issue 9 (January 14, 2016)
| Page Range | 1954-1955 | |
| FR Document | 2016-00595 |
[Federal Register Volume 81, Number 9 (Thursday, January 14, 2016)] [Notices] [Pages 1954-1955] From the Federal Register Online [www.thefederalregister.org] [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: [email protected]. 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
![1954 Federal Register / Vol. 81, No. 9 / Thursday, January 14, 2016 / Notices
Each PRC is housed within an projects conducted separate from their The CDC currently funds 26 PRCs.
accredited school of public health or an core projects or SIP research. Structured Each PRC will annually report the
accredited school of medicine or telephone interviews with key PRC required information to the CDC. The
osteopathy with a preventive medicine informants allow PRC Program staff to annualized estimated burden is
residency program. The PRCs conduct collect indicator data that do not lend expected to increase. This increase
outcomes-oriented, applied prevention themselves to a survey-based equates to an estimated weekly burden
research on a broad range of topics methodology and require a qualitative of one hour per respondent and more
using a multi-disciplinary and approach. fully accounts for the burden of
community-engaged approach. Each CDC requests OMB approval to revise preparing responses, as well as the
PRC receives funding from the CDC to the information collection plan as burden of reporting responses. Web-
establish its core infrastructure and follows: based data collection will occur on an
functions and support a core research annual basis. The KIIs will take place in
(1) The content of the web-based survey
project. In addition to core research
will be updated to more closely align with 2016 and 2018. This equates to two PRC
projects, most PRCs are awarded revised evaluation indicators. In addition, the Network KIIs per PRC Program awardee
funding to complete special interest web-based survey will be migrated from a
projects (SIPs) and conduct other during the three year OMB approval
third party platform to a web-based data period. Responses are annualized in the
research projects. collection system hosted on CDC servers.
The DP14–001 program Although the estimated burden per response burden table below.
announcement included language that will increase, the revised data collection The proposed web-based data
was used to develop and operationalize system will be comprehensive and will collection system will allow data entry
a set of 25 PRC Program evaluation reduce the need for follow-up clarification by during the entire year, which will
indicators. The PRC Program logic PRC Program awardees.
enable respondents to distribute burden
model identifies program inputs, (2) CDC will discontinue telephone
interviews and conduct key informant throughout each funding year. Response
activities, outputs, and outcomes. The burden is expected to decrease in
interviews (KII) every other year to capture
list of indicators was revised to better qualitative information about PRC Network funding years 2 through 5, since the
reflect program needs and capture PRCs’ formation and cohesion. web-based data collection system will
center and research activities, outputs, replicate a number of data elements
and outcomes. CDC will continue to use the
from year-to-year, and respondents will
The CDC is currently approved to information reported by PRCs to
only need to enter changes.
collect information from the PRCs identify training and technical
through a structured telephone assistance needs, respond to requests for OMB approval is requested for three
interview and a web-based survey information from Congress and other years. CDC plans to implement revised
hosted by a third-party. The web-based sources, monitor grantees’ compliance reporting requirements in March 2016.
survey is designed to collect with cooperative agreement PRC Program awardees are required to
information on the PRCs’ collaborations requirements, evaluate progress made in participate in information collection.
with health departments; formal achieving goals and objectives, and There are no costs to respondents other
training programs and other training describe the impact and effectiveness of than their time. The total estimated
activities; and other-funded research the PRC Program. annualized burden hours are 1,299.
ESTIMATED ANNUALIZED BURDEN HOURS
Average
Number of
Number of burden per
Type of respondent Form name responses per
respondents response
respondent (in hrs.)
Prevention Research Center .. Web-based Data Collection ................................................... 26 1 48
Key Informant Interview: PRCs Network ............................... 17 1 3
Leroy A. Richardson, DEPARTMENT OF HEALTH AND 2017. This plan will contain the
Chief, Information Collection Review Office, HUMAN SERVICES description of how the grantee intends
Office of Scientific Integrity, Office of the to structure, measure and evaluate the
Associate Director for Science, Office of the Administration for Children and implementation of the project.
Director, Centers for Disease Control and Families Information contained in this
Prevention. Implementation Plan will enable the
[FR Doc. 2016–00563 Filed 1–13–16; 8:45 am] [OMB No. 0970–0410] Program Office to provide the necessary
BILLING CODE 4163–18–P Proposed Information Collection technical assistance to help ensure that
Activity; Comment Request grantees are structuring Tribal PREP
projects within the framework of PREP
Title: Tribal PREP Implementation design guidance, including mandated
Plan. adult preparation subjects, Positive
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Description: This request to collect Youth Development and evidence-based
information for the Tribal PREP programming.
Implementation Plan, is due by July 1, Respondents:
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![Federal Register / Vol. 81, No. 9 / Thursday, January 14, 2016 / Notices 1955
ANNUAL BURDEN ESTIMATES
Number of Average
Number of Total burden
Instrument responses per burden hours
respondents hours
respondent per response
Tribal PREP Plan ............................................................................................. 10 1 40 400
Estimated Total Annual Burden ACTION: Notice of public workshop; third party may not wish to be posted,
Hours: 400. request for comments. such as medical information, your or
In compliance with the requirements anyone else’s Social Security number, or
of Section 3506(c)(2)(A) of the SUMMARY: The Food and Drug confidential business information, such
Paperwork Reduction Act of 1995, the Administration (FDA) is announcing the as a manufacturing process. Please note
Administration for Children and following public workshop entitled that if you include your name, contact
Families is soliciting public comment ‘‘Patient and Medical Professional information, or other information that
on the specific aspects of the Perspectives on the Return of Genetic identifies you in the body of your
information collection described above. Test Results.’’ The purpose of this comments, that information will be
Copies of the proposed collection of public workshop is to understand posted on http://www.regulations.gov.
information can be obtained and patient and provider perspectives on • If you want to submit a comment
comments may be forwarded by writing receiving potentially medically relevant with confidential information that you
to the Administration for Children and genetic test results. The topic(s) to be do not wish to be made available to the
Families, Office of Administration, discussed will focus on better defining public, submit the comment as a
Office of Information Services, 370 the specific information patients and written/paper submission and in the
L’Enfant Promenade SW., Washington, providers prefer to receive, with an manner detailed (see ‘‘Written/Paper
DC 20447, Attn: ACF Reports Clearance emphasis on the type(s) and amount of Submissions’’ and ‘‘Instructions’’).
Officer. Email address: infocollection@ evidence available to interpret the
acf.hhs.gov. All requests should be results for medical purposes, how those Written/Paper Submissions
identified by the title of the information results should be returned, and what Submit written/paper submissions as
collection. information is needed to understand the follows:
The Department specifically requests results in the event that they could • Mail/Hand delivery/Courier (for
comments on: (a) whether the proposed effectively aid in medical decision written/paper submissions): Division of
collection of information is necessary making. Dockets Management (HFA–305), Food
for the proper performance of the DATES: The public workshop will be and Drug Administration, 5630 Fishers
functions of the agency, including held on March 2, 2016, from 8 a.m. to Lane, Rm. 1061, Rockville, MD 20852.
whether the information shall have 4 p.m. Submit either electronic or • For written/paper comments
practical utility; (b) the accuracy of the written comments on the public submitted to the Division of Dockets
agency’s estimate of the burden of the workshop by March 31, 2016. Management, FDA will post your
proposed collection of information; (c) ADDRESSES: The public workshop will comment, as well as any attachments,
the quality, utility, and clarity of the be held at FDA’s White Oak Campus, except for information submitted,
information to be collected; and (d) 10903 New Hampshire Ave., Bldg. 31 marked and identified, as confidential,
ways to minimize the burden of the Conference Center, the Great Room (Rm. if submitted as detailed in
collection of information on 1503), Silver Spring, MD 20993. ‘‘Instructions.’’
respondents, including through the use Entrance for the public meeting Instructions: All submissions received
of automated collection techniques or participants (non-FDA employees) is must include the Docket No. FDA–
other forms of information technology. through Building 1, where routine 2015–N–4809 for ‘‘Patient and Medical
Consideration will be given to security check procedures will be Professional Perspectives on the Return
comments and suggestions submitted performed. For parking and security of Genetic Test Results; Public
within 60 days of this publication. information, please refer to http://www. Workshop; Request for Comments.’’
Robert Sargis, fda.gov/AboutFDA/WorkingatFDA/ Received comments will be placed in
Reports Clearance Officer. BuildingsandFacilities/WhiteOak the docket and, except for those
CampusInformation/ucm241740.htm. submitted as ‘‘Confidential
[FR Doc. 2016–00595 Filed 1–13–16; 8:45 am]
You may submit comments as Submissions,’’ publicly viewable at
BILLING CODE 4184–01–P
follows: http://www.regulations.gov or at the
Division of Dockets Management
Electronic Submissions between 9 a.m. and 4 p.m., Monday
DEPARTMENT OF HEALTH AND
HUMAN SERVICES Submit electronic comments in the through Friday.
following way: • Confidential Submissions—To
Food and Drug Administration • Federal eRulemaking Portal: http:// submit a comment with confidential
www.regulations.gov. Follow the information that you do not wish to be
[Docket No. FDA–2015–N–4809] instructions for submitting comments. made publicly available, submit your
mstockstill on DSK4VPTVN1PROD with NOTICES
Comments submitted electronically, comments only as a written/paper
Patient and Medical Professional
including attachments, to http:// submission. You should submit two
Perspectives on the Return of Genetic
www.regulations.gov will be posted to copies total. One copy will include the
Test Results and Interpretations;
the docket unchanged. Because your information you claim to be confidential
Public Workshop; Request for
comment will be made public, you are with a heading or cover note that states
Comments
solely responsible for ensuring that your ‘‘THIS DOCUMENT CONTAINS
AGENCY: Food and Drug Administration, comment does not include any CONFIDENTIAL INFORMATION’’. The
HHS. confidential information that you or a Agency will review this copy, including
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Document Created: 2016-01-14 02:51:02
Document Modified: 2016-01-14 02:51:02
| Category | Regulatory Information | |
| Collection | Federal Register | |
| sudoc Class | AE 2.7: GS 4.107: AE 2.106: | |
| Publisher | Office of the Federal Register, National Archives and Records Administration | |
| Section | Notices | |
| FR Citation | 81 FR 1954 |
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