Agency Information Collection Activities: Submission for OMB Review; Comment Request, 4031-4032 [2022-01495]
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Federal Register / Vol. 87, No. 17 / Wednesday, January 26, 2022 / Notices
pursuant to the Authority’s racetrack
safety rules; or
(3) Prohibit a Racetrack from
conducting any Covered Horserace.
By direction of the Commission.
Joel Christie,
Acting Secretary.
8370. Final Civil Sanction
BILLING CODE 6750–01–P
[FR Doc. 2022–01663 Filed 1–25–22; 8:45 am]
Any decision rendered by the Board
of the Authority under Rule 8350, or the
Authority under Rule 8360, shall
constitute a final civil sanction subject
to appeal and review in accordance with
the provisions of 15 U.S.C. 3058.
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8400. Investigatory Powers
(a) The Commission, the Authority, or
their designees:
(1) Shall have free access to the books,
records, offices, racetrack facilities, and
other places of business of Covered
Persons that are used in the care,
treatment, training, and racing of
Covered Horses, and to the books,
records, offices, facilities, and other
places of business of any person who
owns a Covered Horse or performs
services on a Covered Horse; and
(2) May seize any medication, drug,
substance, paraphernalia, object, or
device in violation or suspected
violation of any provision of 15 U.S.C.
57A or the regulations of the Authority.
(b) A Covered Person shall:
(1) Cooperate with the Commission,
the Authority or their designees during
any investigation; and
(2) Respond truthfully to the best of
the Covered Person’s knowledge if
questioned by the Commission, the
Authority, or their designees about a
racing matter.
(c) A Covered Person or any officer,
employee or agent of a Covered Person
shall not hinder a person who is
conducting an investigation under or
attempting to enforce or administer any
provision of 15 U.S.C. 57A or the
regulations of the Authority.
(d) The Commission or the Authority
may issue subpoenas for the attendance
of witnesses in proceedings within their
jurisdiction and for the production of
documents, records, papers, books,
supplies, devices, equipment, and all
other instrumentalities related to
matters within the jurisdiction of the
Commission or the Authority.
(e) Failure to comply with a subpoena
or with the other provisions of this Rule
may be penalized by the imposition of
one or more penalties set forth in Rule
8200.
(f) The Commission or the Authority
may administer oaths to witnesses and
require witnesses to testify under oath
in matters within the jurisdiction of the
Commission or the Authority.
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17:34 Jan 25, 2022
Jkt 256001
GENERAL SERVICES
ADMINISTRATION
Information Collection; General
Services Administration Regulation;
Packing List Clause
Office of Acquisition Policy,
General Services Administration (GSA).
ACTION: Notice and request for
comments.
AGENCY:
Under the provisions of the
Paperwork Reduction Act of 1995, GSA
invites the public to comment on a
request to review and approve an
extension of a previously approved
information collection requirement
regarding the packing list clause.
DATES: Submit comments on or before:
March 28, 2022.
ADDRESSES: Submit comments
identified by Information Collection
3090–0246 via https://
www.regulations.gov. Submit comments
via the Federal eRulemaking portal by
searching the OMB control number.
Select the link ‘‘Submit a Comment’’
that corresponds with ‘‘Information
Collection 3090–0246, Packing List
Clause’’. Follow the instructions
provided at the ‘‘Submit a Comment’’
screen. Please include your name,
company name (if any), and
‘‘Information Collection 3090–0246,
Packing List Clause’’ on your attached
document.
Instructions: Please submit comments
only and cite Information Collection
3090–0246, Packing List Clause, in all
correspondence related to this
collection. Comments received generally
will be posted without change to https://
www.regulations.gov, including any
personal and/or business confidential
information provided. To confirm
receipt of your comment(s), please
check www.regulations.gov,
approximately two-to-three days after
submission to verify posting.
FOR FURTHER INFORMATION CONTACT: Mr.
Clarence Harrison Jr, Procurement
Analyst, at telephone 202–227–7051, or
via email at gsarpolicy@gsa.gov.
SUPPLEMENTARY INFORMATION:
SUMMARY:
A. Purpose
GSAR clause 552.211–77, Packing
List, requires a contractor to include a
Frm 00068
Fmt 4703
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packing list or other suitable document
that verifies placement of an order and
identifies the items shipped. In addition
to information contractors would
normally include on packing lists, the
identification of cardholder name,
telephone number and the term ‘‘Credit
Card’’ is required.
B. Annual Reporting Burdens
[OMB Control No. 3090–0246; Docket No.
2022–0001; Sequence No. 1]
PO 00000
4031
Respondents: 14,923.
Responses per Respondent: 19.
Total Annual Responses: 283,233.
Hours per Response: .05.
Total Burden Hours: 14,161.
C. Public Comments
Public comments are particularly
invited on: Whether this collection of
information is necessary and whether it
will have practical utility; whether our
estimate of the public burden of this
collection of information is accurate and
based on valid assumptions and
methodology; ways to enhance the
quality, utility, and clarity of the
information to be collected.
Obtaining Copies of Proposals:
Requesters may obtain a copy of the
information collection documents from
the GSA Regulatory Secretariat Division,
by calling 202–501–4755 or emailing
GSARegSec@gsa.gov.
Jeffrey A. Koses,
Senior Procurement Executive, Office of
Acquisition Policy, Office of Governmentwide Policy.
[FR Doc. 2022–01490 Filed 1–25–22; 8:45 am]
BILLING CODE 6820–61–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Centers for Medicare & Medicaid
Services
[Document Identifier: CMS–10157 and CMS–
R–262]
Agency Information Collection
Activities: Submission for OMB
Review; Comment Request
Centers for Medicare &
Medicaid Services, Health and Human
Services (HHS).
ACTION: Notice.
AGENCY:
The Centers for Medicare &
Medicaid Services (CMS) is announcing
an opportunity for the public to
comment on CMS’ intention to collect
information from the public. Under the
Paperwork Reduction Act of 1995
(PRA), federal agencies are required to
publish notice in the Federal Register
concerning each proposed collection of
information, including each proposed
SUMMARY:
E:\FR\FM\26JAN1.SGM
26JAN1
4032
Federal Register / Vol. 87, No. 17 / Wednesday, January 26, 2022 / Notices
extension or reinstatement of an existing
collection of information, and to allow
a second opportunity for public
comment on the notice. Interested
persons are invited to send comments
regarding the burden estimate or any
other aspect of this collection of
information, including the necessity and
utility of the proposed information
collection for the proper performance of
the agency’s functions, the accuracy of
the estimated burden, ways to enhance
the quality, utility, and 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.
Comments on the collection(s) of
information must be received by the
OMB desk officer by February 25, 2022.
ADDRESSES: Written comments and
recommendations for the proposed
information collection should be sent
within 30 days of publication of this
notice to www.reginfo.gov/public/do/
PRAMain. Find this particular
information collection by selecting
‘‘Currently under 30-day Review—Open
for Public Comments’’ or by using the
search function.
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’ website address at
https://www.cms.gov/Regulations-andGuidance/Legislation/Paperwork
ReductionActof1995/PRA-Listing.html.
FOR FURTHER INFORMATION CONTACT:
William Parham at (410) 786–4669.
SUPPLEMENTARY INFORMATION: Under the
Paperwork Reduction Act of 1995 (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 (44 U.S.C.
3506(c)(2)(A)) requires federal agencies
to publish a 30-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
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DATES:
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17:34 Jan 25, 2022
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publishing this notice that summarizes
the following proposed collection(s) of
information for public comment:
1. Type of Information Collection
Request: Extension of a currently
approved collection; Title of
Information Collection: The HIPAA
Eligibility Transaction System (HETS);
Use: CMS created the HETS application
to provide Health Insurance Portability
and Accountability Act of 1996 (HIPAA)
compliant 270/271 health care
eligibility inquiries (270) and responses
(271) on a real-time basis. In creating the
HETS application, federal law requires
that CMS take precautions to minimize
the security risk to federal information
systems. Accordingly, CMS is requiring
that trading partners who wish to
connect to the HETS 270/271
application via the CMS Extranet and/
or internet agree to specific trading
partner terms as a condition of receiving
access to Medicare eligibility
information. Applicants will complete
the entire Trading Partner Agreement
form to indicate agreement with CMS
trading partner terms and provide
sufficient information to establish
connectivity to the service and assure
that those entities that access the
Medicare eligibility information are
aware of applicable provisions and
penalties for the misuse of information.
CMS uses the Trading Partner
Agreement Form to capture certain
information whereby a person certifies
that they are fully aware of any and all
penalties related to the use of PHI and
their access to this data from the HETS
application. The information is an
attestation by the authorized
representative of an entity that wishes to
access the Medicare eligibility
information to conduct real-time
eligibility transactions. The authorized
representative is a person responsible
for business decisions on behalf of the
Organization who is submitting the
access request. The data captured
includes the authorized representative’s
name, title contact number and the
name of the submitting entity. Other
data captured is the submitter’s National
Provider Identifier (NPI), business
name, billing address, physical address,
and telephone number. Form Number:
CMS–10157 (OMB control number:
0938–0960); Frequency: Annually;
Affected Public: Private Sector,
Businesses or other for-profits; Number
of Respondents: 1,000; Total Annual
Responses: 1,000; Total Annual Hours:
250. (For policy questions regarding this
collection contact Rupinder Singh at
410–786–7484.)
PO 00000
Frm 00069
Fmt 4703
Sfmt 4703
2. Type of Information Collection
Request: Revision of a currently
approved collection; Title of
Information Collection: Contract Year
2023 Plan Benefit Package (PBP)
Software and Formulary Submission;
Use: Under the Medicare Modernization
Act (MMA), Medicare Advantage (MA)
and Prescription Drug Plan (PDP)
organizations are required to submit
plan benefit packages for all Medicare
beneficiaries residing in their service
area. The plan benefit package
submission consists of the Plan Benefit
Package (PBP) software, formulary file,
and supporting documentation, as
necessary. MA and PDP organizations
use the PBP software to describe their
organization’s plan benefit packages,
including information on premiums,
cost sharing, authorization rules, and
supplemental benefits. They also
generate a formulary to describe their
list of drugs, including information on
prior authorization, step therapy,
tiering, and quantity limits.
CMS requires that MA and PDP
organizations submit a completed PBP
and formulary as part of the annual
bidding process. During this process,
organizations prepare their proposed
plan benefit packages for the upcoming
contract year and submit them to CMS
for review and approval. CMS uses this
data to review and approve the benefit
packages that the plans will offer to
Medicare beneficiaries. This allows
CMS to review the benefit packages in
a consistent way across all submitted
bids during with incredibly tight
timeframes. This data is also used to
populate data on Medicare Plan Finder,
which allows beneficiaries to access and
compare Medicare Advantage and
Prescription Drug plans. Form Number:
CMS–R–262 (OMB control number:
0938–0763); Frequency: Yearly; Affected
Public: Private sector (Business or other
for-profits and Not-for-profit
institutions), State, Local, or Tribal
Governments; Number of Respondents:
785; Total Annual Responses: 8,405;
Total Annual Hours: 76,378. (For policy
questions regarding this collection
contact Kristy L Holtje at 410–786–
2209.)
Dated: January 21, 2022.
William N. Parham, III,
Director, Paperwork Reduction Staff, Office
of Strategic Operations and Regulatory
Affairs.
[FR Doc. 2022–01495 Filed 1–25–22; 8:45 am]
BILLING CODE 4120–01–P
E:\FR\FM\26JAN1.SGM
26JAN1
]]>Agencies
[Federal Register Volume 87, Number 17 (Wednesday, January 26, 2022)]
[Notices]
[Pages 4031-4032]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2022-01495]
=======================================================================
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DEPARTMENT OF HEALTH AND HUMAN SERVICES
Centers for Medicare & Medicaid Services
[Document Identifier: CMS-10157 and CMS-R-262]
Agency Information Collection Activities: Submission for OMB
Review; Comment Request
AGENCY: Centers for Medicare & Medicaid Services, Health and Human
Services (HHS).
ACTION: Notice.
-----------------------------------------------------------------------
SUMMARY: The Centers for Medicare & Medicaid Services (CMS) is
announcing an opportunity for the public to comment on CMS' intention
to collect information from the public. Under the Paperwork Reduction
Act of 1995 (PRA), federal agencies are required to publish notice in
the Federal Register concerning each proposed collection of
information, including each proposed
[[Page 4032]]
extension or reinstatement of an existing collection of information,
and to allow a second opportunity for public comment on the notice.
Interested persons are invited to send comments regarding the burden
estimate or any other aspect of this collection of information,
including the necessity and utility of the proposed information
collection for the proper performance of the agency's functions, the
accuracy of the estimated burden, ways to enhance the quality, utility,
and 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 on the collection(s) of information must be received by
the OMB desk officer by February 25, 2022.
ADDRESSES: Written comments and recommendations for the proposed
information collection should be sent within 30 days of publication of
this notice to www.reginfo.gov/public/do/PRAMain. Find this particular
information collection by selecting ``Currently under 30-day Review--
Open for Public Comments'' or by using the search function.
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' website address at https://www.cms.gov/Regulations-and-Guidance/Legislation/PaperworkReductionActof1995/PRA-Listing.html.
FOR FURTHER INFORMATION CONTACT: William Parham at (410) 786-4669.
SUPPLEMENTARY INFORMATION: Under the Paperwork Reduction Act of 1995
(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 (44 U.S.C. 3506(c)(2)(A)) requires
federal agencies to publish a 30-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 that
summarizes the following proposed collection(s) of information for
public comment:
1. Type of Information Collection Request: Extension of a currently
approved collection; Title of Information Collection: The HIPAA
Eligibility Transaction System (HETS); Use: CMS created the HETS
application to provide Health Insurance Portability and Accountability
Act of 1996 (HIPAA) compliant 270/271 health care eligibility inquiries
(270) and responses (271) on a real-time basis. In creating the HETS
application, federal law requires that CMS take precautions to minimize
the security risk to federal information systems. Accordingly, CMS is
requiring that trading partners who wish to connect to the HETS 270/271
application via the CMS Extranet and/or internet agree to specific
trading partner terms as a condition of receiving access to Medicare
eligibility information. Applicants will complete the entire Trading
Partner Agreement form to indicate agreement with CMS trading partner
terms and provide sufficient information to establish connectivity to
the service and assure that those entities that access the Medicare
eligibility information are aware of applicable provisions and
penalties for the misuse of information.
CMS uses the Trading Partner Agreement Form to capture certain
information whereby a person certifies that they are fully aware of any
and all penalties related to the use of PHI and their access to this
data from the HETS application. The information is an attestation by
the authorized representative of an entity that wishes to access the
Medicare eligibility information to conduct real-time eligibility
transactions. The authorized representative is a person responsible for
business decisions on behalf of the Organization who is submitting the
access request. The data captured includes the authorized
representative's name, title contact number and the name of the
submitting entity. Other data captured is the submitter's National
Provider Identifier (NPI), business name, billing address, physical
address, and telephone number. Form Number: CMS-10157 (OMB control
number: 0938-0960); Frequency: Annually; Affected Public: Private
Sector, Businesses or other for-profits; Number of Respondents: 1,000;
Total Annual Responses: 1,000; Total Annual Hours: 250. (For policy
questions regarding this collection contact Rupinder Singh at 410-786-
7484.)
2. Type of Information Collection Request: Revision of a currently
approved collection; Title of Information Collection: Contract Year
2023 Plan Benefit Package (PBP) Software and Formulary Submission; Use:
Under the Medicare Modernization Act (MMA), Medicare Advantage (MA) and
Prescription Drug Plan (PDP) organizations are required to submit plan
benefit packages for all Medicare beneficiaries residing in their
service area. The plan benefit package submission consists of the Plan
Benefit Package (PBP) software, formulary file, and supporting
documentation, as necessary. MA and PDP organizations use the PBP
software to describe their organization's plan benefit packages,
including information on premiums, cost sharing, authorization rules,
and supplemental benefits. They also generate a formulary to describe
their list of drugs, including information on prior authorization, step
therapy, tiering, and quantity limits.
CMS requires that MA and PDP organizations submit a completed PBP
and formulary as part of the annual bidding process. During this
process, organizations prepare their proposed plan benefit packages for
the upcoming contract year and submit them to CMS for review and
approval. CMS uses this data to review and approve the benefit packages
that the plans will offer to Medicare beneficiaries. This allows CMS to
review the benefit packages in a consistent way across all submitted
bids during with incredibly tight timeframes. This data is also used to
populate data on Medicare Plan Finder, which allows beneficiaries to
access and compare Medicare Advantage and Prescription Drug plans. Form
Number: CMS-R-262 (OMB control number: 0938-0763); Frequency: Yearly;
Affected Public: Private sector (Business or other for-profits and Not-
for-profit institutions), State, Local, or Tribal Governments; Number
of Respondents: 785; Total Annual Responses: 8,405; Total Annual Hours:
76,378. (For policy questions regarding this collection contact Kristy
L Holtje at 410-786-2209.)
Dated: January 21, 2022.
William N. Parham, III,
Director, Paperwork Reduction Staff, Office of Strategic Operations and
Regulatory Affairs.
[FR Doc. 2022-01495 Filed 1-25-22; 8:45 am]
BILLING CODE 4120-01-P
