ATTACHMENT B. 60 Day Federal Register Notice

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Federal Register / Vol. 83, No. 40 / Wednesday, February 28, 2018 / Notices
Contract-level or Plan-level: (1)
Enrollment and Disenrollment—to
evaluate sponsors’ processing of
enrollment, disenrollment, and
reinstatement requests in accordance
with CMS requirements. (2) Medication
Therapy Management (MTM)
Programs—to evaluate Part D MTM
programs, and sponsors’ adherence to
CMS requirements. (3) Grievances—to
assess sponsors’ compliance with timely
and appropriate resolution of grievances
filed by their enrollees. (4) Improving
Drug Utilization Review Controls—to
determine the impact of formulary-level
edits at point of sale in sponsors’
processing of opioid prescriptions. (5)
Coverage Determinations and
Redeterminations—to assess sponsors’
compliance with appropriate resolution
of coverage determinations and
redeterminations requested by their
enrollees. (6) Employer/Union
Sponsored Sponsors—to ensure PDPs
and the employer groups that contract
with the PDPs properly utilize
appropriate waivers and modifications.
Form Number: CMS–10185 (OMB
control number: 0938–0992); Frequency:
Annually and semi-annually; Affected
Public: Private sector (Business or other
for-profits); Number of Respondents:
627; Total Annual Responses: 13,603;
Total Annual Hours: 14,748. (For policy
questions regarding this collection
contact Chanelle Jones at 410–786–
8008.)
Dated: February 23, 2018.
William N. Parham, III,
Director, Paperwork Reduction Staff, Office
of Strategic Operations and Regulatory
Affairs.
[FR Doc. 2018–04061 Filed 2–27–18; 8:45 am]
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DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Children and
Families
Proposed Information Collection
Activity; Comment Request
Title: Multi-site Implementation
Evaluation of Tribal Home Visiting
(MUSE).
OMB No.: New Collection.
Description: The Administration for
Children and Families (ACF) within the
U.S. Department of Health and Human
Services has launched a national multisite evaluation of Tribal Maternal,
Infant, and Early Childhood Home
Visiting (TMIECHV) programs. MUSE is
the first multi-site, multi-model study
that will systematically explore how
home visiting programs are operating
across diverse tribal contexts and
identify factors that lead to programs’
success. The evaluation will provide
information that will help the federal
government design and support federal
home visiting initiatives in tribal
communities and similar populations.
Evaluation findings will also assist
programs with improving home visiting
services for children and families. The
aims of MUSE are to (1) identify and
describe the primary influences shaping
tribal home visiting program planning;
(2) identify and describe how home
visiting programs are being
implemented; and (3) explore supports
to home visiting implementation in
tribal communities. To address these
aims, the evaluation will gather data
about participating home visiting
programs from program staff and parent
program participants and utilize
administrative program data.
The current Notice is specific to data
collection efforts needed to address the
MUSE aims. Quantitative and
qualitative data will be collected from
program staff and parent program
participants at each program site.
Program sites will also submit local
administrative data to the evaluation
team. After obtaining informed consent
Total number of
respondents

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Instrument
Participant Survey—Baseline ........................................
Participant Survey—6 & 12 Month Follow-up ...............
Family Resources Check-in—Baseline and 12 Month
Follow-up ....................................................................
Rapid Reflect Self-Completed Home Visit Questionnaire for Participants ..................................................
Rapid Reflect Self Completed Home Visit Questionnaire for Home Visitors ..............................................
Home Visitor Survey ......................................................
Program Coordinator/Manager Survey ..........................
Program Director Survey ...............................................

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Annual
number of
respondents

from all respondents, data collection
will include: (1) A survey of parent
program participants at enrollment
(baseline), (2) a follow-up survey of
parent program participants at 6 and 12
months, (3) the MUSE Family Resources
Check-in administered to parent
program participants at baseline and 12
months (4) a Rapid Reflect selfcompleted questionnaire completed by
parent program participants after
selected home visits; (5) a Rapid Reflect
self-completed questionnaire completed
by home visitors after selected home
visits; (6) a one-time survey of home
visitors; (7) a one-time survey of
program coordinators/managers; (8) a
one-time survey of program directors;
(9) a one-time survey of local program
evaluators; (10) qualitative interviews of
home visitors at each site; (11)
qualitative interviews of program
coordinators/managers and program
directors at each site; (12) qualitative
interviews of local program evaluators
at each site; (13) qualitative interviews
of program participants; (14) a log of
implementation activities completed by
program coordinators/managers on
staffing, training, family group
activities, and supervision; and (15)
electronic compilation and submission
of administrative program data.
All data collection will be used to
generate information about how tribal
home visiting program services are
planned and delivered, and about what
individual, organizational, community,
and external factors support successful
program implementation.
Respondents: Parent participants
enrolled in TMIECHV programs and
TMIECHV program staff (program
directors, program coordinators/
managers, home visitors, and local
program evaluators).
Annual Burden Estimates
We will request approval for three
years, which will accommodate an
approximate two-year data collection
period and any potential delays in the
data collection timeline.
Number of
responses per
respondent

Average
burden hours
per response

Annual
burden hours

423
312

141
104

1
2

.25
.50

35
104

354

118

2

.25

59

1,394

1 697

12

.08

669

93
81
21
21

1 47

180
1
1
1

.2
1.17
1
1

1,692
32
7
7

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27
7
7

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8682

Federal Register / Vol. 83, No. 40 / Wednesday, February 28, 2018 / Notices
Total number of
respondents

Instrument
Local Program Evaluator Survey ...................................
Qualitative Interviews of Home Visitors .........................
Qualitative Interviews of Program Coordinators/Managers and Program Directors .....................................
Qualitative Interviews of Local Program Evaluators ......
Qualitative Interviews of Program Participants ..............
Implementation Logs ......................................................
Administrative Program Data .........................................
1 The

Number of
responses per
respondent

Average
burden hours
per response

Annual
burden hours

30
42

10
14

1
1

.5
2

5
28

34
30
51
17
17

11
10
17
19
19

1
1
1
24
4

1.5
1.5
1
.67
45

17
15
17
145
1,620

annual number of respondents is annualized over 2 years for instruments that are completed by respondents on an ongoing basis.

National Committee on Vital and Health
Statistics: Meeting

Health and Human Services (HHS)
announces the following advisory
committee meeting.
Name: National Committee on Vital
and Health Statistics (NCVHS),
Standards Subcommittee Meeting.
Date and Times: Monday, March 26,
2018: 9:00 a.m.–3:30 p.m. (EDT).
Place: Virtual.
Status: Open. There will be an open
comment period during the final 15
minutes of the committee meeting.
Purpose: Health Insurance Portability
and Accountability Act (HIPAA)
legislation from 1996, as amended,1
directed the Secretary of HHS to publish
regulations adopting standards, code
sets and identifiers to support the
exchange of electronic health
information between covered entities.
The standards are for retail pharmacy
and medical transactions. New versions
of the adopted standards may be
brought forward to NCVHS by the
standards development organizations
(SDOs) or through the Designated
Standards Maintenance Organization
(DSMO) after completion of a consensus
based review and evaluation process.
On January 9, 2018, the DSMO
submitted a letter to NCVHS
recommending the adoption of two
National Council of Prescription Drug
Program (NCPDP) updates to the
adopted retail pharmacy standards.
These updates include: (1) An update to
the retail pharmacy standard, the
NCPDP Telecommunication and Batch
standard version D.0., which was
adopted in 2009. The update would be
NCPDP Telecommunication and Batch
standard version F2, which would
enable eligibility verification, claims,
services, information reporting, prior
authorization (for pharmacy), and predetermination of benefits; and (2) an
update to the Medicaid subrogation
standard, also adopted in 2009, to
expand subrogation to all payers,
including Medicare Parts C and D. The
updated subrogation standard is the
Batch Standard version 10, and replaces

Pursuant to the Federal Advisory
Committee Act, the Department of

1 along with Section 1104 (c) of the Affordable
Care Act.

Estimated Total Annual Burden
Hours: 4,452.
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.
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: OPRE
Reports Clearance Officer. Email
address: OPREinfocollection@
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.
Mary Jones,
ACF/OPRE Certifying Officer.
[FR Doc. 2018–04039 Filed 2–27–18; 8:45 am]
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Annual
number of
respondents

DEPARTMENT OF HEALTH AND
HUMAN SERVICES

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version 3.0. It will enable all payers to
conduct a uniform process to support
compliance with requirements for
recovery of federal, state and other plan
overpayments, mitigating manual
processes currently in place.
The purpose of this NCVHS Standards
Subcommittee hearing is to obtain input
from stakeholders for the costs and
benefits of implementing the updated
versions of the two pharmacy standards:
NCPDP F2 and pharmacy subrogation,
and to understand how they would
reduce existing barriers to the use of
standards, or mitigate burdens.
The times and topics are subject to
change. Please refer to the posted
agenda for any updates.
Contact Persons for More Information:
Substantive program information may
be obtained from Rebecca Hines, MHS,
Executive Secretary, NCVHS, National
Center for Health Statistics, Centers for
Disease Control and Prevention, 3311
Toledo Road, Hyattsville, Maryland
20782, telephone (301) 458–4715.
Information pertaining to meeting
content may be obtained from Lorraine
Doo, MSW, MPH, or Geanelle G.
Herring, MSW, Centers for Medicare &
Medicaid Services, Office of Information
Technology, Division of National
Standards, 7500 Security Boulevard,
Baltimore, Maryland, 21244, telephone
(410) 786–6597. Summaries of meetings
and a roster of Committee members are
available on the NCVHS website:
https://www.ncvhs.hhs.gov/, where
further information including an agenda
and instructions to access the live audio
broadcast of the meetings will also be
posted.
Should you require reasonable
accommodation, please contact the CDC
Office of Equal Employment
Opportunity on (770) 488–3210 as soon
as possible.
Dated: February 22, 2018.
Laina Bush,
Deputy Assistant Secretary for Planning and
Evaluation, Office of the Assistant Secretary
for Planning and Evaluation.
[FR Doc. 2018–04057 Filed 2–27–18; 8:45 am]
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