Submission for OMB Review; Comment Request, 42556-42557 [2017-19061]
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42556
Federal Register / Vol. 82, No. 173 / Friday, September 8, 2017 / Notices
clarity of the information to be
collected, and the use of automated
collection techniques or other forms of
information technology to minimize the
information collection burden.
DATES: Comments must be received by
November 7, 2017.
ADDRESSES: When commenting, please
reference the document identifier or
OMB control number. To be assured
consideration, comments and
recommendations must be submitted in
any one of the following ways:
1. Electronically. You may send your
comments electronically to https://
www.regulations.gov. Follow the
instructions for ‘‘Comment or
Submission’’ or ‘‘More Search Options’’
to find the information collection
document(s) that are accepting
comments.
2. By regular mail. You may mail
written comments to the following
address: CMS, Office of Strategic
Operations and Regulatory Affairs,
Division of Regulations Development,
Attention: Document Identifier/OMB
Control Number lll, Room C4–26–
05, 7500 Security Boulevard, Baltimore,
Maryland 21244–1850.
To obtain copies of a supporting
statement and any related forms for the
proposed collection(s) summarized in
this notice, you may make your request
using one of following:
1. Access CMS’ Web site address at
https://www.cms.hhs.gov/Paperwork
ReductionActof1995.
2. Email your request, including your
address, phone number, OMB number,
and CMS document identifier, to
Paperwork@cms.hhs.gov.
3. Call the Reports Clearance Office at
(410) 786–1326.
FOR FURTHER INFORMATION CONTACT:
William Parham at (410) 786–4669.
SUPPLEMENTARY INFORMATION:
Contents
This notice sets out a summary of the
use and burden associated with the
following information collections. More
detailed information can be found in
each collection’s supporting statement
and associated materials (see
ADDRESSES).
CMS–10401 Standards Related to
Reinsurance, Risk Corridors, and Risk
Adjustment
Under the PRA (44 U.S.C. 3501–
3520), federal agencies must obtain
approval from the Office of Management
and Budget (OMB) for each collection of
information they conduct or sponsor.
The term ‘‘collection of information’’ is
defined in 44 U.S.C. 3502(3) and 5 CFR
1320.3(c) and includes agency requests
or requirements that members of the
public submit reports, keep records, or
provide information to a third party.
Section 3506(c)(2)(A) of the PRA
requires federal agencies to publish a
60-day notice in the Federal Register
concerning each proposed collection of
information, including each proposed
extension or reinstatement of an existing
collection of information, before
submitting the collection to OMB for
approval. To comply with this
requirement, CMS is publishing this
notice.
Information Collection
1. Type of Information Collection
Request: Extension of a currently
approved collection; Title of
Information Collection: Standards
Related to Reinsurance, Risk Corridors,
and Risk Adjustment; Use: Extension of
data collection required to run
Reinsurance, Risk Corridors, and Risk
Adjustment programs pending complete
revision in near future to update and
remove obsolete programs; Form
Number: CMS–10401 (OMB control
number: 0938–1155); Frequency:
Annually; Affected Public: Health
Insurance Issuers; Number of
Respondents: 2,400; Total Annual
Responses: 15,600,081,744; Total
Annual Hours: 19,281,600. (For policy
questions regarding this collection
contact Ernest Ayukawa at
410.492.5213.)
Dated: September 5, 2017.
William N. Parham, III,
Director, Paperwork Reduction Staff, Office
of Strategic Operations and Regulatory
Affairs.
[FR Doc. 2017–19060 Filed 9–7–17; 8:45 am]
BILLING CODE 4120–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Children and
Families
Submission for OMB Review;
Comment Request
Administration for Native Americans
(ANA) On-Going Progress Report (OPR)
and Objective Work Plan (OWP).
OMB No.: 0970–0452.
Description: Content changes are
being made to the Objective Progress
Report, now known as the On-going
Progress Report (OPR) previously
approved under information collection
(OMB No. 0980–0204. ANA reduced
and renumbered the OPR questions to
allow for the collection of information
necessary for the ongoing monitoring of
grantee progress and performance of
their grant award. The majority of
information requested from the grantees
is less than previous OPR versions and
includes edits for clarification and
simplification purposes.
The information in the OPR is
collected on a semi-annual basis to
monitor the performance of grantees and
better gauge grantee progress. The semiannual data collection replaces the
previous quarterly filing requirement of
the OPR.
The Objective Work Plan information
collection is conducted in accordance
with 42 U.S.C. of the Native American
Programs Act of 1972, as amended. This
collection is necessary to evaluate
applications for financial assistance and
determine the relative merits of the
projects for which such assistance is
requested, as set forth in Sec. 806 [42
U.S.C. 2991d–1](a)(1).
The Ongoing Progress Report
information collection is conducted in
accordance with Sec. 811 [42 U.S.C.
2992] of the Native American Programs
Act and will allow ANA to report
quantifiable results across all program
areas. It also provides grantees with
parameters for reporting their progress
and helps ANA better monitor and
determine the effectiveness of their
projects.
Respondents:
sradovich on DSK3GMQ082PROD with NOTICES
ANNUAL BURDEN ESTIMATES
Number of
respondents
Instrument
OWP ................................................................................................................
OPR .................................................................................................................
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Number of
responses per
respondent
500
275
E:\FR\FM\08SEN1.SGM
1
2
08SEN1
Average
burden hours
per response
3
1
Total burden
hours
1,500
550
Federal Register / Vol. 82, No. 173 / Friday, September 8, 2017 / Notices
Estimated Total Annual Burden
Hours: 2,050.
Additional Information: Copies of the
proposed collection may be obtained by
writing to the Administration for
Children and Families, Office of
Planning, Research and Evaluation, 330
C Street SW., Washington, DC 20201.
Attention Reports Clearance Officer. All
requests should be identified by the title
of the information collection. Email
address: infocollection@acf.hhs.gov.
OMB Comment: OMB is required to
make a decision concerning the
collection of information between 30
and 60 days after publication of this
document in the Federal Register.
Therefore, a comment is best assured of
having its full effect if OMB receives it
within 30 days of publication. Written
comments and recommendations for the
proposed information collection should
be sent directly to the following: Office
of Management and Budget, Paperwork
Reduction Project, Email: OIRA_
SUBMISSION@OMB.EOP.GOV, Attn:
Desk Officer for the Administration for
Children and Families.
Robert Sargis,
Reports Clearance Officer.
[FR Doc. 2017–19061 Filed 9–7–17; 8:45 am]
BILLING CODE 4184–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2017–N–4790]
Self-Collection Devices for Pap Test;
Public Workshop; Request for
Comments
AGENCY:
Food and Drug Administration,
HHS.
Notice of public workshop;
request for comments.
ACTION:
The Food and Drug
Administration (FDA, the Agency, or
we) is announcing the following public
workshop entitled ‘‘Self-Collection
Devices for Pap Test.’’ The purpose of
the public workshop is to obtain
feedback about the feasibility, benefits,
risks, impact on current standard of
care, and least burdensome validation
approaches for self-collection devices
for cervical samples for the purpose of
cervical cancer screening by Pap testing.
Comments and suggestions generated
through this workshop will guide the
development of an appropriate least
burdensome regulatory framework for
the evaluation of cervical sample selfcollection devices to be used for cervical
cancer screening of patients.
sradovich on DSK3GMQ082PROD with NOTICES
SUMMARY:
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42557
DATES:
Written/Paper Submissions
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’’).
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–4790 for ‘‘Self-Collection
Devices for Pap Test.’’ Received
comments, those filed in a timely
manner (see ADDRESSES), 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
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://
The public workshop will be
held on January 11, 2018, from 9 a.m.
to 4 p.m. Submit either electronic or
written comments on this public
workshop by February 14, 2018.
ADDRESSES: The public workshop will
be held at FDA’s White Oak Campus,
10903 New Hampshire Ave., Building
31 Conference Center, the Great Room
(Rm. 1503), Silver Spring, MD 20993–
0002. Entrance for the public workshop
participants (non-FDA employees) is
through Building 1 where routine
security check procedures will be
performed. For parking and security
information, please refer to https://
www.fda.gov/AboutFDA/Working
atFDA/BuildingsandFacilities/White
OakCampusInformation/
ucm241740.htm. See the
SUPPLEMENTARY INFORMATION section for
registration date and information.
You may submit comments as
follows. Please note that late, untimely
filed comments will not be considered.
Electronic comments must be submitted
on or before February 14, 2018. The
https://www.regulations.gov electronic
filing system will accept comments
until midnight Eastern Time at the end
of February 14, 2018. Comments
received by mail/hand delivery/courier
(for written/paper submissions) will be
considered timely if they are
postmarked or the delivery service
acceptance receipt is on or before that
date.
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Agencies
[Federal Register Volume 82, Number 173 (Friday, September 8, 2017)]
[Notices]
[Pages 42556-42557]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2017-19061]
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Administration for Children and Families
Submission for OMB Review; Comment Request
Administration for Native Americans (ANA) On-Going Progress Report
(OPR) and Objective Work Plan (OWP).
OMB No.: 0970-0452.
Description: Content changes are being made to the Objective
Progress Report, now known as the On-going Progress Report (OPR)
previously approved under information collection (OMB No. 0980-0204.
ANA reduced and renumbered the OPR questions to allow for the
collection of information necessary for the ongoing monitoring of
grantee progress and performance of their grant award. The majority of
information requested from the grantees is less than previous OPR
versions and includes edits for clarification and simplification
purposes.
The information in the OPR is collected on a semi-annual basis to
monitor the performance of grantees and better gauge grantee progress.
The semi-annual data collection replaces the previous quarterly filing
requirement of the OPR.
The Objective Work Plan information collection is conducted in
accordance with 42 U.S.C. of the Native American Programs Act of 1972,
as amended. This collection is necessary to evaluate applications for
financial assistance and determine the relative merits of the projects
for which such assistance is requested, as set forth in Sec. 806 [42
U.S.C. 2991d-1](a)(1).
The Ongoing Progress Report information collection is conducted in
accordance with Sec. 811 [42 U.S.C. 2992] of the Native American
Programs Act and will allow ANA to report quantifiable results across
all program areas. It also provides grantees with parameters for
reporting their progress and helps ANA better monitor and determine the
effectiveness of their projects.
Respondents:
Annual Burden Estimates
----------------------------------------------------------------------------------------------------------------
Number of Average burden
Instrument Number of responses per hours per Total burden
respondents respondent response hours
----------------------------------------------------------------------------------------------------------------
OWP............................................. 500 1 3 1,500
OPR............................................. 275 2 1 550
----------------------------------------------------------------------------------------------------------------
[[Page 42557]]
Estimated Total Annual Burden Hours: 2,050.
Additional Information: Copies of the proposed collection may be
obtained by writing to the Administration for Children and Families,
Office of Planning, Research and Evaluation, 330 C Street SW.,
Washington, DC 20201. Attention Reports Clearance Officer. All requests
should be identified by the title of the information collection. Email
address: infocollection@acf.hhs.gov.
OMB Comment: OMB is required to make a decision concerning the
collection of information between 30 and 60 days after publication of
this document in the Federal Register. Therefore, a comment is best
assured of having its full effect if OMB receives it within 30 days of
publication. Written comments and recommendations for the proposed
information collection should be sent directly to the following: Office
of Management and Budget, Paperwork Reduction Project, Email:
OIRA_SUBMISSION@OMB.EOP.GOV, Attn: Desk Officer for the Administration
for Children and Families.
Robert Sargis,
Reports Clearance Officer.
[FR Doc. 2017-19061 Filed 9-7-17; 8:45 am]
BILLING CODE 4184-01-P