Proposed Information Collection Activity; Comment Request, 52835 [2018-22700]
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52835
Federal Register / Vol. 83, No. 202 / Thursday, October 18, 2018 / Notices
Title: Child Care and Development
Fund (CCDF) State Monitoring
Compliance Demonstration Packet.
OMB No.: New.
Description: The proposed data
collection form is designed as part of the
evidence collection process of the
Onsite Monitoring system and provides
states with an opportunity to propose
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Children and
Families
Proposed Information Collection
Activity; Comment Request
Proposed Projects: Office of Child
Care CCDF Onsite Monitoring.
how they, as block-grant recipients, will
choose to demonstrate compliance.
Respondents: 51 States and Territories
triennially.
ANNUAL BURDEN ESTIMATES
Number of
respondents
Instrument
khammond on DSK30JT082PROD with NOTICES
Compliance Demonstration Chart ....................................................................
Document Submission Chart ...........................................................................
Estimated Total Annual Burden
Hours: 1,632 hours.
In compliance with the requirements
of the Paperwork Reduction Act of 1995
(Pub. L. 104–13, 44 U.S.C. chap 35), 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: 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. 2018–22700 Filed 10–17–18; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2018–D–3443]
Content of Premarket Submissions for
Management of Cybersecurity in
Medical Devices; Draft 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 draft
guidance entitled ‘‘Content of Premarket
Submissions for Management of
Cybersecurity in Medical Devices.’’ As
more medical devices are becoming
interconnected, cybersecurity threats
have become more numerous, more
frequent, more severe, and more
clinically impactful. There is a need to
provide manufacturers with specific
technical recommendations (e.g.,
appropriate threat modeling and other
premarket testing) to help ensure device
cybersecurity. The updates to the
existing ‘‘Content of Premarket
Submissions for Management of
Cybersecurity in Medical Devices’’
guidance is anticipated to better protect
against risks, such as ransomware
campaigns, that could disrupt clinical
operations and delay patient care and
risks, such as exploiting a vulnerability
that enables attacks on multiple
patients. This draft guidance is not final
nor is it in effect at this time.
DATES: Submit either electronic or
written comments on the draft guidance
by March 18, 2019 to ensure that the
Agency considers your comment on this
SUMMARY:
PO 00000
Frm 00036
Fmt 4703
Sfmt 4703
Number of
responses per
respondent
1
1
Average
burden hours
per response
16
80
Total burden
hours
272
1,360
draft guidance before it begins work on
the final version of the guidance.
ADDRESSES: You may submit comments
on any guidance at any time as follows:
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
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): Dockets
Management Staff (HFA–305), Food and
Drug Administration, 5630 Fishers
Lane, Rm. 1061, Rockville, MD 20852.
• For written/paper comments
submitted to the Dockets Management
Staff, FDA will post your comment, as
E:\FR\FM\18OCN1.SGM
18OCN1
]]>Agencies
[Federal Register Volume 83, Number 202 (Thursday, October 18, 2018)]
[Notices]
[Page 52835]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2018-22700]
[[Page 52835]]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Administration for Children and Families
Proposed Information Collection Activity; Comment Request
Proposed Projects: Office of Child Care CCDF Onsite Monitoring.
Title: Child Care and Development Fund (CCDF) State Monitoring
Compliance Demonstration Packet.
OMB No.: New.
Description: The proposed data collection form is designed as part
of the evidence collection process of the Onsite Monitoring system and
provides states with an opportunity to propose how they, as block-grant
recipients, will choose to demonstrate compliance.
Respondents: 51 States and Territories triennially.
Annual Burden Estimates
----------------------------------------------------------------------------------------------------------------
Number of Average burden
Instrument Number of responses per hours per Total burden
respondents respondent response hours
----------------------------------------------------------------------------------------------------------------
Compliance Demonstration Chart.................. 17 1 16 272
Document Submission Chart....................... 17 1 80 1,360
----------------------------------------------------------------------------------------------------------------
Estimated Total Annual Burden Hours: 1,632 hours.
In compliance with the requirements of the Paperwork Reduction Act
of 1995 (Pub. L. 104-13, 44 U.S.C. chap 35), 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: 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. 2018-22700 Filed 10-17-18; 8:45 am]
BILLING CODE 4184-43-P
