Proposed Information Collection Activity; Comment Request, 89468-89469 [2016-29709]
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Federal Register / Vol. 81, No. 238 / Monday, December 12, 2016 / Notices
guidance on statistically appropriate
uses of the data. Participation in the
ACBS is voluntary and there are no
costs to respondents other than their
time. The burden table reflects the
landline and cell phone data collection
collection which is the most recent data
released.
The total estimated annualized
burden hours for all respondents are
6,029 hours.
methods used in 2013 and later years.
Additionally, the burden table accounts
for reporting burden incurred by the
states for the monthly or quarterly data
submission to CDC. The burden hour
estimates represent the 2013 data
ESTIMATED ANNUALIZED BURDEN HOURS
Type of respondents
BRFSS Adults .................................................
BRFSS Parents or Guardians of Children ......
ACBS Adults ...................................................
ACBS Parents or Guardians of Children ........
State BRFSS Coordinators .............................
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.
[FR Doc. 2016–29730 Filed 12–9–16; 8:45 am]
BILLING CODE 4163–18–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Children and
Families
Proposed Information Collection
Activity; Comment Request
Title: Accomplishments of the
Domestic Violence Hotline, Online
Connections and Text (ADVHOCaT)
Study.
OMB No.: 0970–0468.
Description: The National Domestic
Violence Hotline (The Hotline) and
ACBS
ACBS
ACBS
ACBS
ACBS
ACBS
ACBS
Number of
responses per
respondent
Number of
respondents
Form name
Landline Screener—Adult ...................
Cell Phone Screener—Adult ...............
Landline Screener—Child ...................
Cell Phone Screener—Child ...............
Adult Consent and Survey—2013 ......
Child Consent and Survey—2013 ......
Data Submission Layout .....................
loveisrespect (LIR), which are supported
by the Division of Family Violence
Prevention and Services within the
Family and Youth Services Bureau
(FYSB) of the Administration for
Children and Families (ACF), U.S.
Department of Health and Human
Services (HHS), serve as partners in the
intervention, prevention, and resource
assistance efforts of the network of
domestic violence and dating violence
service providers.
In order to describe the activities and
accomplishments of The Hotline and
LIR and develop potential new or
revised performance measures, the ACF/
HHS Office of Planning, Research and
Evaluation (OPRE) and FYSB are
proposing a data collection activity as
part of the Accomplishments of the
Domestic Violence Hotline, Online
Connections and Text (ADVHOCaT)
Study.
As part of ongoing program activities
and monitoring for The Hotline and LIR,
21,424
8,976
4,245
2,238
19,954
3,887
40
1
1
1
1
1
1
12
Average
burden per
response
(in hrs.)
1/60
1/60
1/60
1/60
10/60
10/60
3
ACF proposes to collect information via
voluntary phone, chat, and web-based
surveys of individuals who contact The
Hotline and LIR. Participants will
complete a baseline survey at the end of
their contact with The Hotline and LIR,
and a follow-up survey approximately
two weeks later. The survey will
include questions about reasons for
contacting The Hotline/LIR, whether
needs were met, satisfaction with
services received, and helpfulness of
information provided. This data
collection builds on a previous data
collection that was focused on
understanding the preferred mode of
contact by those who contact The
Hotline and LIR. This new information
will inform future efforts to monitor and
improve the performance of domestic
violence hotlines and provide hotline
services.
Respondents: Individuals aged 18 and
older who contact The Hotline and LIR
via phone or chat.
ANNUAL BURDEN ESTIMATES—2 YEAR REQUEST
Total
number of
respondents
Instrument
mstockstill on DSK3G9T082PROD with NOTICES
The Hotline/LIR Baseline Survey .........................................
The Hotline/LIR Follow Up Survey ......................................
Estimated Total Annual Burden
Hours: 172.
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
VerDate Sep<11>2014
18:59 Dec 09, 2016
Jkt 241001
Annual
number of
respondents
2200
2200
1100
1100
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: OPREinfocollection@
acf.hhs.gov. All requests should be
identified by the title of the information
collection.
PO 00000
Frm 00044
Fmt 4703
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Number of
responses per
respondent
1
1
Average
burden hours
per response
0.056
0.1
Annual
burden hours
62
110
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)
E:\FR\FM\12DEN1.SGM
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Federal Register / Vol. 81, No. 238 / Monday, December 12, 2016 / Notices
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 Jones,
Reports Clearance Officer.
[FR Doc. 2016–29709 Filed 12–9–16; 8:45 am]
BILLING CODE 4184–32–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2016–D–3466]
Immediately in Effect Guidance
Document: Conditions for Sale for AirConduction Hearing Aids; Guidance
for Industry and Food and Drug
Administration Staff; Availability
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice of availability.
The Food and Drug
Administration (FDA or Agency) is
announcing the availability of the
guidance entitled ‘‘Immediately in
Effect Guidance Document: Conditions
for Sale for Air-Conduction Hearing
Aids.’’ FDA is issuing this guidance to
communicate to consumers, hearing aid
dispensers, hearing aid manufacturers,
and hearing health professionals that
FDA does not intend to enforce certain
conditions for sale of hearing aid
devices that are required per FDA
regulation. Specifically, FDA does not
intend to enforce the medical evaluation
or recordkeeping requirements prior to
the dispensing of certain hearing aid
devices to individuals 18 years of age
and older.
DATES: Submit either electronic or
written comments on this guidance at
any time. General comments on Agency
guidance documents are welcome at any
time.
ADDRESSES: You may submit comments
as follows:
SUMMARY:
mstockstill on DSK3G9T082PROD with NOTICES
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
VerDate Sep<11>2014
18:59 Dec 09, 2016
Jkt 241001
solely responsible for ensuring that your
comment does not include any
confidential information that you or a
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–
2016–D–3466 for ‘‘Immediately in Effect
Guidance Document: Conditions for
Sale for Air-Conduction Hearing Aids.’’
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
the claimed confidential information, in
its consideration of comments. The
second copy, which will have the
claimed confidential information
redacted/blacked out, will be available
for public viewing and posted on https://
www.regulations.gov. Submit both
PO 00000
Frm 00045
Fmt 4703
Sfmt 4703
89469
copies to the Division of Dockets
Management. If you do not wish your
name and contact information to be
made publicly available, you can
provide this information on the cover
sheet and not in the body of your
comments and you must identify this
information as ‘‘confidential.’’ Any
information marked as ‘‘confidential’’
will not be disclosed except in
accordance with 21 CFR 10.20 and other
applicable disclosure law. For more
information about FDA’s posting of
comments to public dockets, see 80 FR
56469, September 18, 2015, or access
the information at: https://www.fda.gov/
regulatoryinformation/dockets/
default.htm.
Docket: For access to the docket to
read background documents or the
electronic and written/paper comments
received, go to https://
www.regulations.gov and insert the
docket number, found in brackets in the
heading of this document, into the
‘‘Search’’ box and follow the prompts
and/or go to the Division of Dockets
Management, 5630 Fishers Lane, Rm.
1061, Rockville, MD 20852.
An electronic copy of the guidance
document is available for download
from the Internet. See the
SUPPLEMENTARY INFORMATION section for
information on electronic access to the
guidance. Submit written requests for a
single hard copy of the guidance
document entitled ‘‘Immediately in
Effect Guidance Document: Conditions
for Sale for Air-Conduction Hearing
Aids’’ to the Office of the Center
Director, Guidance and Policy
Development, Center for Devices and
Radiological Health, Food and Drug
Administration, 10903 New Hampshire
Ave., Bldg. 66, Rm. 5431, Silver Spring,
MD 20993–0002. Send one selfaddressed adhesive label to assist that
office in processing your request.
FOR FURTHER INFORMATION CONTACT:
Srinivas Nandkumar, Center for Devices
and Radiological Health, Food and Drug
Administration, 10903 New Hampshire
Ave., Bldg. 66, Rm. 2436, Silver Spring,
MD 20993–0002, 301–796–6480.
SUPPLEMENTARY INFORMATION:
I. Background
FDA is issuing this guidance to
communicate to consumers, hearing aid
dispensers, hearing aid manufacturers,
and hearing health professionals that
FDA does not intend to enforce certain
conditions for sale of hearing aid
devices that are required per FDA
regulation. Specifically, FDA does not
intend to enforce the medical evaluation
(§ 801.421(a) (21 CFR 801.421(a)) or
recordkeeping (§ 801.421(d))
E:\FR\FM\12DEN1.SGM
12DEN1
]]>Agencies
[Federal Register Volume 81, Number 238 (Monday, December 12, 2016)]
[Notices]
[Pages 89468-89469]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2016-29709]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Administration for Children and Families
Proposed Information Collection Activity; Comment Request
Title: Accomplishments of the Domestic Violence Hotline, Online
Connections and Text (ADVHOCaT) Study.
OMB No.: 0970-0468.
Description: The National Domestic Violence Hotline (The Hotline)
and loveisrespect (LIR), which are supported by the Division of Family
Violence Prevention and Services within the Family and Youth Services
Bureau (FYSB) of the Administration for Children and Families (ACF),
U.S. Department of Health and Human Services (HHS), serve as partners
in the intervention, prevention, and resource assistance efforts of the
network of domestic violence and dating violence service providers.
In order to describe the activities and accomplishments of The
Hotline and LIR and develop potential new or revised performance
measures, the ACF/HHS Office of Planning, Research and Evaluation
(OPRE) and FYSB are proposing a data collection activity as part of the
Accomplishments of the Domestic Violence Hotline, Online Connections
and Text (ADVHOCaT) Study.
As part of ongoing program activities and monitoring for The
Hotline and LIR, ACF proposes to collect information via voluntary
phone, chat, and web-based surveys of individuals who contact The
Hotline and LIR. Participants will complete a baseline survey at the
end of their contact with The Hotline and LIR, and a follow-up survey
approximately two weeks later. The survey will include questions about
reasons for contacting The Hotline/LIR, whether needs were met,
satisfaction with services received, and helpfulness of information
provided. This data collection builds on a previous data collection
that was focused on understanding the preferred mode of contact by
those who contact The Hotline and LIR. This new information will inform
future efforts to monitor and improve the performance of domestic
violence hotlines and provide hotline services.
Respondents: Individuals aged 18 and older who contact The Hotline
and LIR via phone or chat.
Annual Burden Estimates--2 Year Request
----------------------------------------------------------------------------------------------------------------
Number of Average burden
Instrument Total number Annual number responses per hours per Annual burden
of respondents of respondents respondent response hours
----------------------------------------------------------------------------------------------------------------
The Hotline/LIR Baseline Survey. 2200 1100 1 0.056 62
The Hotline/LIR Follow Up Survey 2200 1100 1 0.1 110
----------------------------------------------------------------------------------------------------------------
Estimated Total Annual Burden Hours: 172.
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:
OPREinfocollection@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)
[[Page 89469]]
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 Jones,
Reports Clearance Officer.
[FR Doc. 2016-29709 Filed 12-9-16; 8:45 am]
BILLING CODE 4184-32-P
