Proposed Information Collection Activity; Procedures for Requests From Tribal Lead Agencies To Use Child Care and Development Fund (CCDF) Funds for Construction or Major Renovation of Child Care Facilities (OMB #0970-0160), 19080-19081 [2019-09045]
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19080
Federal Register / Vol. 84, No. 86 / Friday, May 3, 2019 / Notices
• The Data Quality Plan update
required pursuant to § 1355.52(d)(5).
The CCWIS regulations require
updates of this information to confirm
that the project meets CCWIS
requirements and that project costs are
appropriately allocated to benefiting
programs.
Respondents: Title IV–E agencies
under the Social Security Act.
ANNUAL BURDEN ESTIMATES
Number of
respondents
Instrument
Automated Function List § 1355.52(i)(2) .........................................................
Data Quality Plan § 1355.52(d)(5) ...................................................................
Estimated Total Annual Burden
Hours: 2,750.
Comments: 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.
Authority: 42 U.S.C. 620 et seq., 42 U.S.C.
670 et seq., 42 U.S.C. 1301 and 1302.
Mary B. Jones,
ACF/OPRE Certifying Officer.
[FR Doc. 2019–09044 Filed 5–2–19; 8:45 am]
BILLING CODE 4184–25–P
Number of
responses per
respondent
55
55
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Children and
Families
Proposed Information Collection
Activity; Procedures for Requests
From Tribal Lead Agencies To Use
Child Care and Development Fund
(CCDF) Funds for Construction or
Major Renovation of Child Care
Facilities (OMB #0970–0160)
Office of Child Care;
Administration for Children and
Families; HHS.
ACTION: Request for public comment.
AGENCY:
The Administration for
Children and Families (ACF) is
requesting proposed revisions with a
three-year extension to an approved
information collection: Procedures for
Requests from Tribal Lead Agencies to
use Child Care and Development Fund
(CCDF) Funds for Construction or Major
Renovation of Child Care Facilities
(OMB #: 0970–0160, expiration date:
9/30/2019).
DATES: Comments due within 60 days of
publication. 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.
ADDRESSES: Copies of the proposed
collection of information can be
SUMMARY:
1
1
Average
burden hours
per response
10
40
Annual burden
hours
550
2,200
obtained and comments may be
forwarded by emailing infocollection@
acf.hhs.gov. Alternatively, copies can
also be obtained 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. All requests,
emailed or written, should be identified
by the title of the information collection.
SUPPLEMENTARY INFORMATION:
Description: The Child Care and
Development Block Grant Act, as
amended, allows federally-recognized
Tribes to use Child Care and
Development Fund (CCDF) grant awards
for construction and renovation of child
care facilities. A tribal grantee must first
request and receive approval from the
Administration for Children and
Families (ACF) before using CCDF funds
for construction or major renovation.
This information collection contains the
statutorily-mandated uniform
procedures for the solicitation and
consideration of requests, including
instructions for preparation of
environmental assessments in
conjunction with the National
Environmental Policy Act. The
proposed draft procedures update the
procedures that were originally issued
in August 1997 (and revised
periodically) by making minor technical
and formatting changes.
Respondents: CCDF tribal grantees
requesting to use CCDF funds for
construction or major renovation.
ANNUAL BURDEN ESTIMATES
Total
number of
respondents
Instrument
amozie on DSK9F9SC42PROD with NOTICES
Construction or Major Renovation of Tribal Child Care Facilities ...................
Estimated Total Annual Burden
Hours: 1,000.
Comments: The Department
specifically requests comments on (a)
whether the proposed collection of
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50
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
PO 00000
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Number of
responses per
respondent
1
Average
burden hours
per response
20
Annual burden
hours
1,000
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
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Federal Register / Vol. 84, No. 86 / Friday, May 3, 2019 / Notices
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.
Authority: Act, 42 U.S.C. 9858(c)(6).
Mary B. Jones,
ACF/OPRE Certifying Officer.
[FR Doc. 2019–09045 Filed 5–2–19; 8:45 am]
BILLING CODE 4184–81–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2017–N–5925]
21st Century Cures Act: Annual
Compilation of Notices of Updates
From the Susceptibility Test
Interpretive Criteria Web Page;
Request for Comments
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
Notice; request for comments.
The Food and Drug
Administration (FDA, the Agency, or
we) is announcing the availability of the
Agency’s annual compilation of notices
of updates to the Agency’s
Susceptibility Test Interpretive Criteria
web page. The Agency established the
Susceptibility Test Interpretive Criteria
web page on December 13, 2017, and
since establishment has provided
updates to both the format of the web
pages and to the susceptibility test
interpretive criteria identified and
recognized by FDA on the web pages.
FDA is publishing this notice in
accordance with procedures established
by the 21st Century Cures Act (Cures
Act).
DATES: This notice is published in the
Federal Register on May 3, 2019.
ADDRESSES: You may submit either
electronic or written comments and
information as follows:
amozie on DSK9F9SC42PROD with NOTICES
SUMMARY:
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,
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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
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–
2017–N–5925 for ‘‘Susceptibility Test
Interpretive Criteria Recognized and
Listed on the Susceptibility Test
Interpretive web page; Request for
Comments.’’ 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
Dockets Management Staff 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 copies to the Dockets Management
Staff. If you do not wish your name and
contact information to be made publicly
available, you can provide this
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19081
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.gpo.gov/
fdsys/pkg/FR-2015-09-18/pdf/201523389.pdf.
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 Dockets Management
Staff, 5630 Fishers Lane, Rm. 1061,
Rockville, MD 20852.
FOR FURTHER INFORMATION CONTACT:
Katherine Schumann, Center for Drug
Evaluation and Research, Food and
Drug Administration, 10903 New
Hampshire Ave., Bldg. 22, Rm. 6242,
Silver Spring, MD 20993–0002, 301–
796–1182, Katherine.Schumann@
fda.hhs.gov.
SUPPLEMENTARY INFORMATION:
I. Background
Section 511A of the Federal Food,
Drug, and Cosmetic Act (the FD&C Act)
(21 U.S.C. 360a–2), as added by section
3044 of the Cures Act (Pub. L. 114–255),
was signed into law on December 13,
2016. This provision clarifies FDA’s
authority to identify and efficiently
update susceptibility test interpretive
criteria, including through the
recognition by FDA of standards
established by standards development
organizations (SDOs). It also clarifies
that sponsors of antimicrobial
susceptibility testing devices may rely
upon listed susceptibility test
interpretive criteria to support
premarket authorization of their
devices, provided they meet certain
conditions, which allows for a more
streamlined process for incorporating
up-to-date information into such
devices.
In the Federal Register notice of
December 13, 2017 (82 FR 58617), FDA
announced the establishment of the
Susceptibility Test Interpretive Criteria
web page. This web page recognizes
susceptibility test interpretive criteria
established by an SDO that fulfills the
requirements under section
511A(b)(2)(A) of the FD&C Act;
identifies when FDA does not recognize,
in whole or in part, susceptibility test
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]]>Agencies
[Federal Register Volume 84, Number 86 (Friday, May 3, 2019)]
[Notices]
[Pages 19080-19081]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2019-09045]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Administration for Children and Families
Proposed Information Collection Activity; Procedures for Requests
From Tribal Lead Agencies To Use Child Care and Development Fund (CCDF)
Funds for Construction or Major Renovation of Child Care Facilities
(OMB #0970-0160)
AGENCY: Office of Child Care; Administration for Children and Families;
HHS.
ACTION: Request for public comment.
-----------------------------------------------------------------------
SUMMARY: The Administration for Children and Families (ACF) is
requesting proposed revisions with a three-year extension to an
approved information collection: Procedures for Requests from Tribal
Lead Agencies to use Child Care and Development Fund (CCDF) Funds for
Construction or Major Renovation of Child Care Facilities (OMB #: 0970-
0160, expiration date: 9/30/2019).
DATES: Comments due within 60 days of publication. 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.
ADDRESSES: Copies of the proposed collection of information can be
obtained and comments may be forwarded by emailing
[email protected]. Alternatively, copies can also be obtained
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. All requests, emailed or
written, should be identified by the title of the information
collection.
SUPPLEMENTARY INFORMATION:
Description: The Child Care and Development Block Grant Act, as
amended, allows federally-recognized Tribes to use Child Care and
Development Fund (CCDF) grant awards for construction and renovation of
child care facilities. A tribal grantee must first request and receive
approval from the Administration for Children and Families (ACF) before
using CCDF funds for construction or major renovation. This information
collection contains the statutorily-mandated uniform procedures for the
solicitation and consideration of requests, including instructions for
preparation of environmental assessments in conjunction with the
National Environmental Policy Act. The proposed draft procedures update
the procedures that were originally issued in August 1997 (and revised
periodically) by making minor technical and formatting changes.
Respondents: CCDF tribal grantees requesting to use CCDF funds for
construction or major renovation.
Annual Burden Estimates
----------------------------------------------------------------------------------------------------------------
Number of Average burden
Instrument Total number responses per hours per Annual burden
of respondents respondent response hours
----------------------------------------------------------------------------------------------------------------
Construction or Major Renovation of Tribal Child 50 1 20 1,000
Care Facilities................................
----------------------------------------------------------------------------------------------------------------
Estimated Total Annual Burden Hours: 1,000.
Comments: 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
[[Page 19081]]
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.
Authority: Act, 42 U.S.C. 9858(c)(6).
Mary B. Jones,
ACF/OPRE Certifying Officer.
[FR Doc. 2019-09045 Filed 5-2-19; 8:45 am]
BILLING CODE 4184-81-P
