83 FR 22688 - Proposed Information Collection Activity; Comment Request
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Administration for Children and Families Federal Register Volume 83, Issue 95 (May 16, 2018)
Administration for Children and Families
Federal Register Volume 83, Issue 95 (May 16, 2018)
| Page Range | 22688-22689 | |
| FR Document | 2018-10461 |
[Federal Register Volume 83, Number 95 (Wednesday, May 16, 2018)] [Notices] [Pages 22688-22689] From the Federal Register Online [www.thefederalregister.org] [FR Doc No: 2018-10461] ======================================================================= ----------------------------------------------------------------------- DEPARTMENT OF HEALTH AND HUMAN SERVICES Administration for Children and Families Proposed Information Collection Activity; Comment Request Title: Evaluation of the Transitional Living Program (TLP). OMB No.: 0970-0383. Description: The Family and Youth Services Bureau (FYSB) and the Office of Planning, Research, Evaluation (OPRE) in the Administration for Children and Families (ACF) are requesting to continue collecting data as part of a currently approved information collection (OMB No. 0970-0383). The purpose is to continue baseline data collection at study enrollment and follow-up data collection for the Evaluation of the Transitional Living Program (TLP). The TLP evaluation was designed to examine the effects of FYSB's Transitional Living Program on runaway and homeless youth, focusing on such outcomes as housing and homelessness, education or training, employment, social connections, socio-emotional well-being, and risk behaviors. Data collection will include three primary surveys, previously approved by OMB: (1) A survey administered at the time of TLP enrollment (baseline), (2) a survey administered 6 months after enrollment, which will collect information on short-terms outcomes; and (3) a survey administered at 12 months, which will collect information on longer-term outcomes. Participants will be enrolled through the TLP study sites. Respondents: Runaway and homeless youth ages 16 to 22 who agree to participate in the study upon enrollment into one of the TLP study sites. Annual Burden Estimates ---------------------------------------------------------------------------------------------------------------- Total number Number of Average Instrument of Annual number responses per burden hours Annual burden respondents of respondents respondent per response hours ---------------------------------------------------------------------------------------------------------------- Young Adult Baseline Survey..... 600 200 1 0.62 124 Young Adult 6-Month Follow Up 600 200 1 0.61 122 Survey......................... Young Adult 12-Month Follow Up 600 200 1 0.61 122 Survey......................... ---------------------------------------------------------------------------------------------------------------- Estimated Total Burden Hours: 368. 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 Planning, Research, and Evaluation, 330 C Street SW, Washington, DC 20201, Attn: OPRE Reports Clearance Officer. Email address: [email protected]. All requests should be identified by the title of the information collection. [[Page 22689]] 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. Mary B. Jones, ACF/OPRE Certifying Officer. [FR Doc. 2018-10461 Filed 5-15-18; 8:45 am] BILLING CODE 4184-01-P
![22688 Federal Register / Vol. 83, No. 95 / Wednesday, May 16, 2018 / Notices
valid assumptions and methodology; DATES: The rescission is as of May 16, OMB No.: 0970–0383.
ways to enhance the quality, utility, and 2018. Description: The Family and Youth
clarity of the information to be FOR FURTHER INFORMATION CONTACT: For Services Bureau (FYSB) and the Office
collected; and ways in which we can clarification of content, please contact of Planning, Research, Evaluation
minimize the burden of the collection of Mr. Cy Greenidge, Office of (OPRE) in the Administration for
information on those who are to Government-wide Policy, Office of Children and Families (ACF) are
respond, through the use of appropriate Asset and Transportation Management,
technological collection techniques or requesting to continue collecting data as
at 202–219–2349, or by email at
other forms of information technology. part of a currently approved information
travelpolicy@gsa.gov. Please cite Notice
of FTR Bulletin 18–04. collection (OMB No. 0970–0383). The
OBTAINING COPIES OF PROPOSALS:
Requesters may obtain a copy of the purpose is to continue baseline data
SUPPLEMENTARY INFORMATION: Executive
information collection documents from collection at study enrollment and
Order 13777, Enforcing the Regulatory
the General Services Administration, Reform Agenda, Section 3, paragraph follow-up data collection for the
Regulatory Secretariat Division (MVCB), (d)(ii), states in part, the Regulatory Evaluation of the Transitional Living
1800 F Street NW, Washington, DC Reform Task Force shall attempt to Program (TLP). The TLP evaluation was
20405, telephone 202–501–4755. Please identify regulations that are outdated, designed to examine the effects of
cite OMB Control No. 9000–0035, unnecessary, or ineffective. GSA has FYSB’s Transitional Living Program on
Claims and Appeals, in all conducted a thorough review of all FTR runaway and homeless youth, focusing
correspondence. bulletins on the FTR Travel/Per Diem on such outcomes as housing and
Dated: May 10, 2018. Bulletins website (https://www.gsa.gov/ homelessness, education or training,
Lorin Curit, policy-regulations/regulations/federal- employment, social connections, socio-
travel-regulation/federal-travel- emotional well-being, and risk
Director, Federal Acquisition Policy Division,
Office of Governmentwide Acquisition Policy, regulation-and-related-files#Travel behaviors.
Office of Acquisition Policy, Office of PerDiemBulletins) and determined that Data collection will include three
Governmentwide Policy. some of the Bulletins contain outdated,
primary surveys, previously approved
[FR Doc. 2018–10408 Filed 5–15–18; 8:45 am] duplicative, expired, or inapplicable
by OMB: (1) A survey administered at
content. FTR Bulletin 18–04 lists all
BILLING CODE 6820–EP–P
rescinded bulletins meeting one of the the time of TLP enrollment (baseline),
aforementioned criterion. (2) a survey administered 6 months after
enrollment, which will collect
GENERAL SERVICES Dated: May 11, 2018.
information on short-terms outcomes;
ADMINISTRATION Alexander Kurien, and (3) a survey administered at 12
[Notice–MA–2018–03; Docket No. 2018– Deputy Associate Administrator, Office of months, which will collect information
0002, Sequence No. 7] Asset and Transportation Management,
Office of Government-wide Policy.
on longer-term outcomes. Participants
Rescission of FTR Bulletins will be enrolled through the TLP study
[FR Doc. 2018–10436 Filed 5–15–18; 8:45 am]
sites.
BILLING CODE 6820–14–P
AGENCY: Office of Government-wide Respondents: Runaway and homeless
Policy (OGP), General Services youth ages 16 to 22 who agree to
Administration (GSA).
DEPARTMENT OF HEALTH AND participate in the study upon
ACTION: Notice of Federal Travel
HUMAN SERVICES enrollment into one of the TLP study
Regulation (FTR) Bulletin 18–04, sites.
rescission of FTR Bulletins. Administration for Children and
SUMMARY: GSA is officially rescinding Families
various FTR bulletins to ensure the
Proposed Information Collection
Travel/Per Diem Bulletin section on the
Activity; Comment Request
agency’s FTR website displays only
current information. Agencies’ policies Title: Evaluation of the Transitional
should be updated as warranted. Living Program (TLP).
ANNUAL BURDEN ESTIMATES
Average
Total Annual Number of burden hours Annual burden
Instrument number of number of responses per per hours
respondents respondents respondent response
Young Adult Baseline Survey .............................................. 600 200 1 0.62 124
Young Adult 6-Month Follow Up Survey ............................. 600 200 1 0.61 122
Young Adult 12-Month Follow Up Survey ........................... 600 200 1 0.61 122
sradovich on DSK3GMQ082PROD with NOTICES
Estimated Total Burden Hours: 368. information collection described above. Washington, DC 20201, Attn: OPRE
In compliance with the requirements Copies of the proposed collection of Reports Clearance Officer. Email
of Section 3506(c)(2)(A) of the information can be obtained and address: OPREinfocollection@
Paperwork Reduction Act of 1995, the comments may be forwarded by writing acf.hhs.gov. All requests should be
Administration for Children and to the Administration for Children and identified by the title of the information
Families is soliciting public comment Families, Office of Planning, Research, collection.
on the specific aspects of the and Evaluation, 330 C Street SW,
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![Federal Register / Vol. 83, No. 95 / Wednesday, May 16, 2018 / Notices 22689
The Department specifically requests MD 20993–0002. Answers to commonly based point-of-care and laboratory-based
comments on (a) whether the proposed asked questions including information in vitro diagnostic devices indicated for
collection of information is necessary regarding special accommodations due use as aids in the diagnosis of human
for the proper performance of the to a disability, visitor parking, and immunodeficiency virus (HIV)
functions of the agency, including transportation may be accessed at: infection. The devices that will be
whether the information shall have https://www.fda.gov/Advisory discussed by the Committee during the
practical utility; (b) the accuracy of the Committees/AboutAdvisoryCommittees/ meeting are post-amendment devices
agency’s estimate of the burden of the ucm408555.htm. that currently are classified into class III
proposed collection of information; (c) FOR FURTHER INFORMATION CONTACT: under section 513(f)(1) of the Federal
the quality, utility, and clarity of the Bryan Emery, Division of Scientific Food, Drug, and Cosmetic Act (21 U.S.C.
information to be collected; and (d) Advisors and Consultants, Center for 360c(f)(1)).
ways to minimize the burden of the Biologics Evaluation and Research FDA intends to make background
collection of information on (CBER), Food and Drug Administration, material available to the public
respondents, including through the use 10903 New Hampshire Ave., Bldg. 71, approximately 2 weeks and no later
of automated collection techniques or Rm. 6268, Silver Spring, MD 20993– than 2 business days before the meeting.
other forms of information technology. 0002, 240–402–8054, bryan.emery@ If FDA is unable to post the background
Consideration will be given to fda.hhs.gov; or Joanne Lipkind, Division material on its website prior to the
comments and suggestions submitted of Scientific Advisors and Consultants, meeting, the background material will
within 60 days of this publication. CBER, Food and Drug Administration, be made publicly available at the
10903 New Hampshire Ave., Bldg. 71, location of the advisory committee
Mary B. Jones, meeting, and the background material
Rm. 6270, Silver Spring, MD 20993–
ACF/OPRE Certifying Officer. will be posted on FDA’s website after
0002, 240–402–8106, joanne.lipkind@
[FR Doc. 2018–10461 Filed 5–15–18; 8:45 am]
fda.hhs.gov; or FDA Advisory the meeting. Background material is
BILLING CODE 4184–01–P
Committee Information Line, 1–800– available at https://www.fda.gov/
741–8138 (301–443–0572 in the AdvisoryCommittees/Calendar/
Washington, DC area). A notice in the default.htm. Scroll down to the
DEPARTMENT OF HEALTH AND Federal Register about last minute appropriate advisory committee meeting
HUMAN SERVICES modifications that impact a previously link.
Procedure: Interested persons may
Food and Drug Administration announced advisory committee meeting
present data, information, or views,
cannot always be published quickly
[Docket No. FDA–2018–N–1773] orally or in writing, on issues pending
enough to provide timely notice.
before the committee. Written
Therefore, you should always check the
Blood Products Advisory Committee; submissions may be made to the contact
Agency’s website at https://
Notice of Meeting person on or before July 11, 2018. Oral
www.fda.gov/AdvisoryCommittees/
presentations from the public will be
AGENCY: Food and Drug Administration, default.htm and scroll down to the
scheduled between approximately 2:15
HHS. appropriate advisory committee meeting
p.m. and 3:15 p.m. on July 18, 2018, and
ACTION: Notice. link, or call the advisory committee between 12:30 p.m. and 1:30 p.m. on
information line to learn about possible July 19, 2018. Those individuals
SUMMARY: The Food and Drug modifications before coming to the interested in making formal oral
Administration (FDA) announces a meeting. For those unable to attend in presentations should notify the contact
forthcoming public advisory committee person, the meeting will be also be person and submit a brief statement of
meeting of the Blood Products Advisory available via webcast. The webcast will the general nature of the evidence or
Committee. The general function of the be available at the following link on arguments they wish to present, the
Blood Products Advisory Committee is both days: https://collaboration.fda.gov/ names and addresses of proposed
to provide advice and recommendations bpac0718/. participants, and an indication of the
to the Agency on regulatory issues SUPPLEMENTARY INFORMATION: approximate time requested to make
related to blood and products derived Agenda: On July 18, 2018, the Blood their presentation on or before July 5,
from blood. On the first day of the Products Advisory Committee will meet 2018. Time allotted for each
meeting, the Committee will provide in open session to discuss and provide presentation may be limited. If the
advice regarding bacterial risk control advice regarding bacterial risk control number of registrants requesting to
strategies to enhance the safety and strategies for blood collection speak is greater than can be reasonably
availability of platelets for transfusion. establishments and transfusion services accommodated during the scheduled
On the second day of the meeting, the to enhance the safety and availability of open public hearing session, FDA may
Committee, supplemented with platelets for transfusion. The Committee conduct a lottery to determine the
members from the Microbiology Devices will discuss the available strategies to speakers for the scheduled open public
Panel of the Medical Devices Advisory control the risk of bacterial hearing session. The contact person will
Committee, will function as a medical contamination of platelets with 5-day notify interested persons regarding their
device panel to provide advice and and 7-day dating, including bacterial request to speak by July 6, 2018.
recommendations to the Agency on testing using culture-based devices and Persons attending FDA’s advisory
classification of devices. The meeting rapid bacterial detection devices and committee meetings are advised that the
will be open to the public.
sradovich on DSK3GMQ082PROD with NOTICES
implementation of pathogen reduction Agency is not responsible for providing
DATES: The meeting will be held on July technology. access to electrical outlets.
18, 2018, from 8 a.m. to 5 p.m. and July On July 19, 2018, the Committee will FDA welcomes the attendance of the
19, 2018, from 8 a.m. to 3 p.m. function as a medical device panel. The public at its advisory committee
ADDRESSES: FDA White Oak Campus, Committee will meet in open session to meetings and will make every effort to
10903 New Hampshire Ave., Bldg. 31 discuss and provide advice regarding accommodate persons with disabilities.
Conference Center, the Great Room (Rm. the device reclassification from class III If you require accommodations due to a
1503, sections B and C), Silver Spring, to class II of nucleic acid and serology- disability, please contact Bryan Emery
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Document Created: 2018-11-02 09:13:39
Document Modified: 2018-11-02 09:13:39
| 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 | 83 FR 22688 |
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