Proposed Information Collection Activity; Judicial, Court, and Attorney Measures of Performance (New Collection), 1416-1417 [2022-00238]
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Federal Register / Vol. 87, No. 7 / Tuesday, January 11, 2022 / Notices
CMS–10286 Notice of Research
Exception under the Genetic
Information Nondiscrimination
CMS–10325 Disclosure and
Recordkeeping Requirements for
Grandfathered Health Plans under the
Affordable Care Act
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.
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Information Collection
1. Type of Information Collection
Request: Extension of a currently
approved collection; Title of
Information Collection: Notice of
Research Exception under the Genetic
Information Nondiscrimination Act;
Use: Under the Genetic Information
Nondiscrimination Act of 2008 (GINA),
a plan or issuer may request (but not
require) a genetic test in connection
with certain research activities so long
as such activities comply with specific
requirements, including: (i) The
research complies with 45 CFR part 46
or equivalent federal regulations and
applicable State or local law or
regulations for the protection of human
subjects in research; (ii) the request for
the participant or beneficiary (or in the
case of a minor child, the legal guardian
of such beneficiary) is made in writing
and clearly indicates that compliance
with the request is voluntary and that
non-compliance will have no effect on
eligibility for benefits or premium or
contribution amounts; and (iii) no
genetic information collected or
acquired will be used for underwriting
purposes. The Secretary of Labor or the
Secretary of Health and Human Services
is required to be notified if a group
health plan or health insurance issuer
intends to claim the research exception
permitted under Title I of GINA.
Nonfederal governmental group health
plans and issuers solely in the
individual health insurance market or
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Medigap market will be required to file
with the Centers for Medicare &
Medicaid Services (CMS). The Notice of
Research Exception under the Genetic
Information Nondiscrimination Act is a
model notice that can be completed by
group health plans and health insurance
issuers and filed with either the
Department of Labor or CMS to comply
with the notification requirement. Form
Number: CMS–10286 (OMB control
number: 0938–1077); Frequency:
Occasionally; Affected Public: Private
Sector; State, Local or Tribal
governments; Number of Respondents:
2; Total Annual Responses: 2; Total
Annual Hours: 0.5. For policy questions
regarding this collection contact Usree
Bandyopadhyay at 410–786–6650.
2. Type of Information Collection
Request: Extension of a currently
approved collection; Title of
Information Collection: Disclosure and
Recordkeeping Requirements for
Grandfathered Health Plans under the
Affordable Care Act; Use: Section 1251
of the Affordable Care Act provides that
certain plans and health insurance
coverage in existence as of March 23,
2010, known as grandfathered health
plans, are not required to comply with
certain statutory provisions in the Act.
The final regulations titled ‘‘Final Rules
under the Affordable Care Act for
Grandfathered Plans, Preexisting
Condition Exclusions, Lifetime and
Annual Limits, Rescissions, Dependent
Coverage, Appeals, and Patient
Protections’’ (80 FR 72192, November
18, 2015) require that, to maintain its
status as a grandfathered health plan, a
plan must maintain records
documenting the terms of the plan in
effect on March 23, 2010, and any other
documents that are necessary to verify,
explain or clarify status as a
grandfathered health plan. The plan
must make such records available for
examination upon request by
participants, beneficiaries, individual
policy subscribers, or a state or federal
agency official. A grandfathered health
plan is also required to include a
statement in any summary of benefits
under the plan or health insurance
coverage, that the plan or coverage
believes it is a grandfathered health plan
within the meaning of section 1251 of
the Affordable Care Act, and providing
contact information for participants to
direct questions and complaints. In
addition, a grandfathered group health
plan that is changing health insurance
issuers is required to provide the
succeeding health insurance issuer (and
the succeeding health insurance issuer
must require) documentation of plan
terms (including benefits, cost sharing,
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employer contributions, and annual
limits) under the prior health insurance
coverage sufficient to make a
determination whether the standards of
paragraph § 147.140(g)(1) of the final
regulations are exceeded. It is also
required that, for an insured group
health plan (or a multiemployer plan)
that is a grandfathered plan, the relevant
policies, certificates, or contracts of
insurance, or plan documents must
disclose in a prominent and effective
manner that employers, employee
organizations, or plan sponsors, as
applicable, are required to notify the
issuer (or multiemployer plan) if the
contribution rate changes at any point
during the plan year. Form Number:
CMS–10325 (OMB control number:
0938–1093); Frequency: Occasionally;
Affected Public: Private Sector, State,
Local or Tribal governments; Number of
Respondents: 14,669; Total Annual
Responses: 2,651,523; Total Annual
Hours: 40. For policy questions
regarding this collection contact Usree
Bandyopadhyay at 410–786–6650.
Dated: January 6, 2022.
William N. Parham, III,
Director, Paperwork Reduction Staff, Office
of Strategic Operations and Regulatory
Affairs.
[FR Doc. 2022–00344 Filed 1–10–22; 8:45 am]
BILLING CODE 4120–01–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Administration for Children and
Families
Proposed Information Collection
Activity; Judicial, Court, and Attorney
Measures of Performance (New
Collection)
Children’s Bureau;
Administration for Children and
Families; HHS.
ACTION: Request for public comment.
AGENCY:
The Children’s Bureau,
Administration for Children and
Families (ACF), U.S. Department of
Health and Human Services (HHS), is
proposing to collect data for a new
descriptive study, Judicial, Court, and
Attorney Measures of Performance
(JCAMP).
DATES: Comments due within 60 days of
publication. In compliance with the
Paperwork Reduction Act of 1995, ACF
is soliciting public comment on the
specific aspects of the information
collection described in this notice.
ADDRESSES: You can obtain copies of the
proposed collection of information and
submit comments by emailing
SUMMARY:
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Federal Register / Vol. 87, No. 7 / Tuesday, January 11, 2022 / Notices
infocollection@acf.hhs.gov. Identify all
requests by the title of the information
collection.
SUPPLEMENTARY INFORMATION:
Description: This study will collect
information from Court Improvement
Program (CIP) staff to (1) understand
data capacity and current use of
performance measures and (2) gather
feedback from the performance measure
pilot process. This will be accomplished
using two instruments:
JCAMP CIP Data Capacity Survey
The survey asks CIPs about their
current capacity to collect specific data
elements from the following six
categories of measurement: (1) Legal and
judicial context (e.g., court docketing),
(2) Practices (e.g., attorney pre-petition
legal practice), (3) Short-term outcomes
that happen during hearings (e.g.,
discussion of key issues), (4)
Intermediate outcomes that happen
during the case (e.g., judicial
continuity), (5) Long-term outcomes that
happen after case closure (e.g., child
safety), and (6) Cross-cutting themes
(e.g., equity). The survey asks about
capacity broadly and then specifically
for a series of subcategories.
JCAMP Pilot Site Debrief Form
The JCAMP Pilot Site Debrief Form is
a survey developed to be administered
to CIP staff who have assisted with
piloting of the performance measures.
The survey asks participants about the
challenges and successes in collecting
pilot data for the measures, their
confidence in collecting the data going
forward, and suggestions for improving
future efforts.
Respondents: Respondents include
CIP Administrators and staff.
ANNUAL BURDEN ESTIMATES
Total
number of
respondents
Instrument
JCAMP CIP Data Capacity Survey .....................................
JCAMP Pilot Debrief Form ..................................................
Estimated Total Annual Burden
Hours: 94.
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: Section 5106, Public Law
111–320, the Child Abuse Prevention
and Treatment Act Reauthorization Act
of 2010, and titles IV–B and IV–E of the
Social Security Act.
Mary B. Jones,
ACF/OPRE Certifying Officer.
[FR Doc. 2022–00238 Filed 1–10–22; 8:45 am]
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Total
number of
responses per
respondent
106
24
1
1
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Food and Drug Administration
[Docket No. FDA–2022–D–0053]
Notifying the Food and Drug
Administration of a Permanent
Discontinuance or Interruption in
Manufacturing of a Device Under
Section 506J of the Federal Food,
Drug, and Cosmetic Act; Draft
Guidance for Industry and Food and
Drug Administration Staff; Availability
AGENCY:
Food and Drug Administration,
HHS.
ACTION:
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264
18
Annual
burden hours
88
6
emergency. FDA is issuing this guidance
to implement amendments to the FD&C
Act by the Coronavirus Aid, Relief, and
Economic Security Act (CARES Act), as
it relates to device shortages and
potential device shortages during or in
advance of a public health emergency.
This draft guidance is not final nor is it
in effect at this time.
Submit either electronic or
written comments on the draft guidance
by March 14, 2022 to ensure that the
Agency considers your comment on this
draft guidance before it begins work on
the final version of the guidance.
DATES:
You may submit comments
on any guidance at any time as follows:
The Food and Drug
Administration (FDA or Agency) is
announcing the availability of the draft
guidance entitled ‘‘Notifying FDA of a
Permanent Discontinuance or
Interruption in Manufacturing of a
Device Under Section 506J of the FD&C
Act.’’ The Federal Food, Drug, and
Cosmetic Act (FD&C Act) requires
manufacturers to notify FDA of a
permanent discontinuance in the
manufacture of certain devices or an
interruption in the manufacture of
certain devices that is likely to lead to
a meaningful disruption in supply of
that device in the United States. This
guidance is intended to assist
manufacturers in providing timely,
informative notifications about changes
in the production of certain medical
device products that will help prevent
or mitigate shortages of such devices
during or in advance of a public health
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.83
.25
Total
burden hours
ADDRESSES:
Notice of availability.
SUMMARY:
Average
burden hours
per response
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
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]]>Agencies
[Federal Register Volume 87, Number 7 (Tuesday, January 11, 2022)]
[Notices]
[Pages 1416-1417]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2022-00238]
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Administration for Children and Families
Proposed Information Collection Activity; Judicial, Court, and
Attorney Measures of Performance (New Collection)
AGENCY: Children's Bureau; Administration for Children and Families;
HHS.
ACTION: Request for public comment.
-----------------------------------------------------------------------
SUMMARY: The Children's Bureau, Administration for Children and
Families (ACF), U.S. Department of Health and Human Services (HHS), is
proposing to collect data for a new descriptive study, Judicial, Court,
and Attorney Measures of Performance (JCAMP).
DATES: Comments due within 60 days of publication. In compliance with
the Paperwork Reduction Act of 1995, ACF is soliciting public comment
on the specific aspects of the information collection described in this
notice.
ADDRESSES: You can obtain copies of the proposed collection of
information and submit comments by emailing
[[Page 1417]]
[email protected]. Identify all requests by the title of the
information collection.
SUPPLEMENTARY INFORMATION:
Description: This study will collect information from Court
Improvement Program (CIP) staff to (1) understand data capacity and
current use of performance measures and (2) gather feedback from the
performance measure pilot process. This will be accomplished using two
instruments:
JCAMP CIP Data Capacity Survey
The survey asks CIPs about their current capacity to collect
specific data elements from the following six categories of
measurement: (1) Legal and judicial context (e.g., court docketing),
(2) Practices (e.g., attorney pre-petition legal practice), (3) Short-
term outcomes that happen during hearings (e.g., discussion of key
issues), (4) Intermediate outcomes that happen during the case (e.g.,
judicial continuity), (5) Long-term outcomes that happen after case
closure (e.g., child safety), and (6) Cross-cutting themes (e.g.,
equity). The survey asks about capacity broadly and then specifically
for a series of subcategories.
JCAMP Pilot Site Debrief Form
The JCAMP Pilot Site Debrief Form is a survey developed to be
administered to CIP staff who have assisted with piloting of the
performance measures. The survey asks participants about the challenges
and successes in collecting pilot data for the measures, their
confidence in collecting the data going forward, and suggestions for
improving future efforts.
Respondents: Respondents include CIP Administrators and staff.
Annual Burden Estimates
----------------------------------------------------------------------------------------------------------------
Total number Average burden
Instrument Total number of responses hours per Total burden Annual burden
of respondents per respondent response hours hours
----------------------------------------------------------------------------------------------------------------
JCAMP CIP Data Capacity Survey.. 106 1 .83 264 88
JCAMP Pilot Debrief Form........ 24 1 .25 18 6
----------------------------------------------------------------------------------------------------------------
Estimated Total Annual Burden Hours: 94.
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: Section 5106, Public Law 111-320, the Child Abuse
Prevention and Treatment Act Reauthorization Act of 2010, and titles
IV-B and IV-E of the Social Security Act.
Mary B. Jones,
ACF/OPRE Certifying Officer.
[FR Doc. 2022-00238 Filed 1-10-22; 8:45 am]
BILLING CODE 4184-29-P
