Final 30 Day FRN

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Federal Register / Vol. 85, No. 37 / Tuesday, February 25, 2020 / Notices

discrimination. The Exchange is
responsible for ensuring that QHPs meet
these minimum certification standards
as described in the Exchange rule under
45 CFR 155 and 156, based on the
Affordable Care Act, as well as other
standards determined by the Exchange.
The reporting requirements and data
collection in the Exchange rule address
Federal requirements that various
entities must meet with respect to the
establishment and operation of an
Exchange; minimum requirements that
health insurance issuers must meet with
respect to participation in a State based
or Federally-facilitated Exchange; and
requirements that employers must meet
with respect to participation in the
SHOP and compliance with other
provisions of the Affordable Care Act.
Form Number: CMS–10593 (OMB
Control Number: 0938–1312) Frequency:
Monthly, Annual; Affected Public:
Private Sector; Number of Respondents:
20; Number of Responses: 361; Total
Annual Hours: 51,805. For policy
questions regarding this collection
contact Courtney Williams at 301–492–
5157.
2. Type of Information Collection
Request: Revision of a currently
approved collection; Title of
Information Collection: End Stage Renal
Disease Annual Facility Survey Form;
Use: The ESRD Program Management
and Medical Information System
(PMMIS) Facility Certification/Survey
Record contains provider-specific and
aggregate patient population data on
beneficiaries treated by that provider
obtained from the Annual Facility
Survey form (CMS–2744). The Facility
Certification portion of the record
captures certification and other
information about ESRD facilities
approved by Medicare to provide
kidney dialysis and transplant services.
The Facility Survey portion of the
record captures activities performed
during the calendar year as well as
aggregate year-end population counts
for both Medicare beneficiaries and nonMedicare patients. The survey includes
the collection on hemodialysis patients
dialyzing more than 4 times per week,
vocational rehabilitation and staffing.
The aggregate patient information is
collected from each Medicare-approved
provider of dialysis and kidney
transplant services. The information is
used to assess and evaluate the local,
regional and national levels of medical
and social impact of ESRD care and is
used extensively by researchers and
suppliers of services for trend analysis.
Form Number: CMS–2744 (OMB control
number: 0938–0447); Frequency: Yearly;
Affected Public: Business or other for-

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profit, Not-for-profit institutions;
Number of Respondents: 7,828; Total
Annual Responses: 7,828; Total Annual
Hours: 31,312. (For policy questions
regarding this collection contact
Gequincia Polk at 410–786–2305)
3. Type of Information Collection
Request: Extension of a currently
approved collection; Title of
Information Collection: Virtual Groups
for Merit-Based Incentive Payment
System (MIPS); Use: CMS acknowledges
the unique challenges that small
practices and practices in rural areas
may face with the implementation of the
Quality Payment Program. To help
support these practices and provide
them with additional flexibility, CMS
has created a virtual group reporting
option starting with the 2018 MIPS
performance period. CMS held webinars
and small, interactive feedback sessions
to gain insight from clinicians as we
developed our policies regarding virtual
groups. During these sessions,
participants expressed a strong interest
in virtual groups, and indicated that the
right policies could minimize clinician
burden and bolster clinician success.
This information collection request is
related to the statutorily required virtual
group election process finalized in the
CY 2018 Quality Payment Program final
rule. A virtual group is a combination of
Tax Identification Numbers (TINs),
which would include at least two
separate TINs associated with a solo
practitioner TIN and National Provider
Identifier (TIN/NPI) or group with 10 or
fewer MIPS eligible clinicians and
another solo practitioner (TIN/NPI) or
group with 10 or fewer MIPS eligible
clinicians.
Section 1848(q)(5)(I) of the Act
requires that CMS establish and have in
place a process to allow an individual
MIPS eligible clinician or group
consisting of not more than 10 MIPS
eligible clinicians to elect, with respect
to a performance period for a year to be
in a virtual group with at least one other
such individual MIPS eligible clinician
or group. The Act also provides for the
use of voluntary virtual groups for
certain assessment purposes, including
the election of practices to be a virtual
group and the requirements for the
election process.
Section 1848(q)(5)(I)(i) of the Act also
provides that MIPS eligible clinicians
electing to be a virtual group must: (1)
Have their performance assessed for all
four performance categories in a manner
that applies the combined performance
of all the MIPS eligible clinicians in the
virtual group to each MIPS eligible
clinician in the virtual group for the
applicable performance period; and (2)

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be scored for all four performance
categories based on such assessment.
CMS will use the data collected from
virtual group representatives to
determine eligibility to participate in a
virtual group, approve the formation of
that virtual group, based on
determination of each TIN size, and
assign a virtual group identifier to the
virtual group. The data collected will
also be used to assign a performance
score to each TIN/NPI in the virtual
group. Form Number: CMS–10652
(OMB control number: 0938–1343);
Frequency: Annually; Affected Public:
Private Sector: Business or other forprofits and Not-for-profit institutions
and Individuals; Number of
Respondents: 16; Total Annual
Responses: 16; Total Annual Hours:
160. (For policy questions regarding this
collection, contact Michelle Peterman at
410–786–2591.)
Dated: February 19, 2020.
William N. Parham, III,
Director, Paperwork Reduction Staff, Office
of Strategic Operations and Regulatory
Affairs.
[FR Doc. 2020–03634 Filed 2–24–20; 8:45 am]
BILLING CODE 4120–01–P

DEPARTMENT OF HEALTH AND
HUMAN SERVICES
[Document Identifier: OS–0990–0452]

Agency Information Collection
Request; 30-Day Public Comment
Request
Office of the Secretary, HHS.
Notice.

AGENCY:
ACTION:

In compliance with the
requirement of the Paperwork
Reduction Act of 1995, the Office of the
Secretary (OS), Department of Health
and Human Services, is publishing the
following summary of a proposed
collection for public comment.
DATES: Comments on the ICR must be
received on or before March 26, 2020.
ADDRESSES: Submit your comments to
OIRA_submission@omb.eop.gov or via
facsimile to (202) 395–5806.
FOR FURTHER INFORMATION CONTACT:
Sherrette Funn, Sherrette.Funn@hhs.gov
or (202) 795–7714. When submitting
comments or requesting information,
please include the document identifier
0990–0452–30D and project title for
reference.
SUMMARY:

Interested
persons are invited to send comments
regarding this burden estimate or any
other aspect of this collection of
information, including any of the

SUPPLEMENTARY INFORMATION:

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Federal Register / Vol. 85, No. 37 / Tuesday, February 25, 2020 / Notices
following subjects: (1) The necessity and
utility of the proposed information
collection for the proper performance of
the agency’s functions; (2) the accuracy
of the estimated burden; (3) ways to
enhance the quality, utility, and clarity
of the information to be collected; and
(4) the use of automated collection
techniques or other forms of information
technology to minimize the information
collection burden.
Title of the Collection: Federal
Evaluation of Making Proud Choices!
(MPC!).
Type of Collection: Revision.
OMB No. 0990–0452.
Abstract: The Office of Population
Affairs (OPA), U.S. Department of
Health and Human Services (HHS) is
requesting an extension with revision of

a currently approved information
collection (OMB No: 0990–0452). The
purpose of the revision is to complete
the nine-month follow-up data
collection for the Federal Evaluation of
Making Proud Choices! (MPC). The
evaluation is being conducted in 15
schools across four school districts
nationwide and will provide
information about program design,
implementation, and impacts through a
rigorous assessment of a highly popular
teen pregnancy prevention
curriculum—MPC. Clearance is
requested for three years. This revision
is necessary to complete the 9-month
post-baseline follow up data collection
after enrolling a fourth and final cohort
into the study. The follow-up survey

data will be used to determine program
effectiveness by comparing sexual
behavior outcomes, such as postponing
sexual activity, and reducing or
preventing sexual risk behaviors and
STDs and intermediate outcomes, such
as improving exposure, knowledge and
attitudes between treatment (program)
and control youth. The findings from
these analyses of program impacts will
be of interest to the general public, to
policymakers, and to schools and other
organizations interested in supporting a
comprehensive approach to teen
pregnancy prevention. The revision
request also updates the burden by
removing the second (15 months post
baseline) survey from the data
collection.

ESTIMATED ANNUALIZED BURDEN TABLE
Number of
respondents

Type of respondent

Average
burden
per response
(in hours)

Total
burden hours

Youth participants ............................................................................................

200

1

30/60

100

Total ..........................................................................................................

........................

1

........................

100

Dated: February 19, 2020.
Terry Clark,
Asst Paperwork Reduction Act Reports
Clearance Officer, Office of the Secretary.
[FR Doc. 2020–03716 Filed 2–24–20; 8:45 am]
BILLING CODE 4150–34–P

DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Meeting of the Secretary’s Advisory
Committee on Human Research
Protections
Department of Health and
Human Services, Office of the Secretary,
Office of the Assistant Secretary for
Health.
ACTION: Notice.
AGENCY:

Pursuant to Section 10(a) of
the Federal Advisory Committee Act,
U.S.C. Appendix 2, notice is hereby
given that the Secretary’s Advisory
Committee on Human Research
Protections (SACHRP) will hold a
meeting that will be open to the public.
Information about SACHRP and the full
meeting agenda will be posted on the
SACHRP website at: http://
www.dhhs.gov/ohrp/sachrp-committee/
meetings/index.html.
DATES: The meeting will be held on
Wednesday, March 11, 2020, from 11
a.m. until 4 p.m., and Thursday, March
12, 2020, from 11 a.m. until 4 p.m.
SUMMARY:

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Number of
responses
per
respondent

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(times are tentative and subject to
change). The confirmed times and
agenda will be posted at https://cmsdrupal-hhs-ohrp-prod.cloud.hhs.gov/
ohrp/sachrp-committee/meetings/
index.html when this information
becomes available.
ADDRESSES: This meeting will be held
via webcast. Members of the public may
also attend the meeting via webcast.
Instructions for attending via webcast
will be posted about one week prior to
the meeting at https://cms-drupal-hhsohrp-prod.cloud.hhs.gov/ohrp/sachrpcommittee/meetings/index.html
FOR FURTHER INFORMATION CONTACT: Julia
Gorey, J.D., Executive Director,
SACHRP; U.S. Department of Health
and Human Services, 1101 Wootton
Parkway, Suite 200, Rockville,
Maryland 20852; telephone: 240–453–
8141; fax: 240–453–6909; email address:
SACHRP@hhs.gov.
SUPPLEMENTARY INFORMATION: Under the
authority of 42 U.S.C. 217a, Section 222
of the Public Health Service Act, as
amended, SACHRP was established to
provide expert advice and
recommendations to the Secretary of
Health and Human Services, through
the Assistant Secretary for Health, on
issues and topics pertaining to or
associated with the protection of human
research subjects.
The Subpart A Subcommittee (SAS)
was established by SACHRP in October

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2006 and is charged with developing
recommendations for consideration by
SACHRP regarding the application of
subpart A of 45 CFR part 46 in the
current research environment.
The Subcommittee on Harmonization
(SOH) was established by SACHRP at its
July 2009 meeting and charged with
identifying and prioritizing areas in
which regulations and/or guidelines for
human subjects research adopted by
various agencies or offices within HHS
would benefit from harmonization,
consistency, clarity, simplification and/
or coordination.
The SACHRP meeting will open to the
public at 11 a.m., on Wednesday, March
11, 2020, followed by opening remarks
from Dr. Jerry Menikoff, Director of
OHRP and Dr. Stephen Rosenfeld,
SACHRP Chair. The meeting will focus
on regulatory and ethical issues
surrounding Deceased Donor
Intervention Research, with a particular
focus on recipient informed consent. An
additional agenda topic will be a
discussion of ethical and regulatory
issues surrounding re-consent of
subjects for humans subjects research.
Other topics will be addressed. For the
full meeting agenda, see https://cmsdrupal-hhs-ohrp-prod.cloud.hhs.gov/
ohrp/sachrp-committee/meetings/
index.html
The public will have an opportunity
to comment to the SACHRP during the
meeting’s public comment session or by

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