83 FR 52835 - Proposed Information Collection Activity; Comment Request
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Administration for Children and Families Federal Register Volume 83, Issue 202 (October 18, 2018)
Administration for Children and Families
Federal Register Volume 83, Issue 202 (October 18, 2018)
| Page Range | 52835-52835 | |
| FR Document | 2018-22700 |
[Federal Register Volume 83, Number 202 (Thursday, October 18, 2018)] [Notices] [Page 52835] From the Federal Register Online [www.thefederalregister.org] [FR Doc No: 2018-22700] [[Page 52835]] ----------------------------------------------------------------------- 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: 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] BILLING CODE 4184-43-P
![Federal Register / Vol. 83, No. 202 / Thursday, October 18, 2018 / Notices 52835
DEPARTMENT OF HEALTH AND Title: Child Care and Development how they, as block-grant recipients, will
HUMAN SERVICES Fund (CCDF) State Monitoring choose to demonstrate compliance.
Compliance Demonstration Packet. Respondents: 51 States and Territories
Administration for Children and
OMB No.: New. triennially.
Families
Description: The proposed data
Proposed Information Collection collection form is designed as part of the
Activity; Comment Request evidence collection process of the
Onsite Monitoring system and provides
Proposed Projects: Office of Child
Care CCDF Onsite Monitoring. states with an opportunity to propose
ANNUAL BURDEN ESTIMATES
Number of Average
Number of Total burden
Instrument responses per burden hours
respondents hours
respondent per response
Compliance Demonstration Chart .................................................................... 17 1 16 272
Document Submission Chart ........................................................................... 17 1 80 1,360
Estimated Total Annual Burden DEPARTMENT OF HEALTH AND draft guidance before it begins work on
Hours: 1,632 hours. HUMAN SERVICES the final version of the guidance.
In compliance with the requirements ADDRESSES: You may submit comments
Food and Drug Administration on any guidance at any time as follows:
of the Paperwork Reduction Act of 1995
(Pub. L. 104–13, 44 U.S.C. chap 35), the Electronic Submissions
Administration for Children and [Docket No. FDA–2018–D–3443]
Submit electronic comments in the
Families is soliciting public comment Content of Premarket Submissions for following way:
on the specific aspects of the Management of Cybersecurity in • Federal eRulemaking Portal: https://
information collection described above. Medical Devices; Draft Guidance for www.regulations.gov. Follow the
Copies of the proposed collection of Industry and Food and Drug instructions for submitting comments.
information can be obtained and Administration Staff; Availability Comments submitted electronically,
comments may be forwarded by writing including attachments, to https://
to the Administration for Children and AGENCY: Food and Drug Administration, www.regulations.gov will be posted to
Families, Office of Planning, Research HHS. the docket unchanged. Because your
and Evaluation, 330 C Street SW, ACTION: Notice of availability. comment will be made public, you are
Washington DC 20201. Attn: ACF solely responsible for ensuring that your
Reports Clearance Officer. Email SUMMARY: The Food and Drug
comment does not include any
Administration (FDA or Agency) is
address: infocollection@acf.hhs.gov. All confidential information that you or a
announcing the availability of the draft
requests should be identified by the title third party may not wish to be posted,
guidance entitled ‘‘Content of Premarket
of the information collection. such as medical information, your or
Submissions for Management of
The Department specifically requests anyone else’s Social Security number, or
Cybersecurity in Medical Devices.’’ As
confidential business information, such
comments on: (a) Whether the proposed more medical devices are becoming
as a manufacturing process. Please note
collection of information is necessary interconnected, cybersecurity threats
that if you include your name, contact
for the proper performance of the have become more numerous, more
information, or other information that
functions of the agency, including frequent, more severe, and more
identifies you in the body of your
whether the information shall have clinically impactful. There is a need to
comments, that information will be
practical utility; (b) the accuracy of the provide manufacturers with specific
posted on https://www.regulations.gov.
agency’s estimate of the burden of the technical recommendations (e.g., • If you want to submit a comment
proposed collection of information; (c) appropriate threat modeling and other with confidential information that you
the quality, utility, and clarity of the premarket testing) to help ensure device do not wish to be made available to the
information to be collected; and (d) cybersecurity. The updates to the public, submit the comment as a
ways to minimize the burden of the existing ‘‘Content of Premarket written/paper submission and in the
collection of information on Submissions for Management of manner detailed (see ‘‘Written/Paper
respondents, including through the use Cybersecurity in Medical Devices’’ Submissions’’ and ‘‘Instructions’’).
guidance is anticipated to better protect
of automated collection techniques or
against risks, such as ransomware Written/Paper Submissions
other forms of information technology.
campaigns, that could disrupt clinical Submit written/paper submissions as
Consideration will be given to
operations and delay patient care and follows:
comments and suggestions submitted risks, such as exploiting a vulnerability • Mail/Hand delivery/Courier (for
khammond on DSK30JT082PROD with NOTICES
within 60 days of this publication. that enables attacks on multiple written/paper submissions): Dockets
Robert Sargis, patients. This draft guidance is not final Management Staff (HFA–305), Food and
Reports Clearance Officer. nor is it in effect at this time. Drug Administration, 5630 Fishers
[FR Doc. 2018–22700 Filed 10–17–18; 8:45 am] DATES: Submit either electronic or Lane, Rm. 1061, Rockville, MD 20852.
BILLING CODE 4184–43–P
written comments on the draft guidance • For written/paper comments
by March 18, 2019 to ensure that the submitted to the Dockets Management
Agency considers your comment on this Staff, FDA will post your comment, as
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Document Created: 2018-10-18 03:05:37
Document Modified: 2018-10-18 03:05:37
| 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 52835 |
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