Administrative Simplification: Modifications of Health Insurance Portability and Accountability Act of 1996 (HIPAA) National Council for Prescription Drug Programs (NCPDP) Retail Pharmacy Standards; and Modification of the Medicaid Pharmacy Subrogation Standard; Delay of Effective Date, 9289-9290 [2025-02511]
Download as PDF
Federal Register / Vol. 90, No. 27 / Tuesday, February 11, 2025 / Rules and Regulations
(4) This AD requires replacing Note 1 of
EASA AD 2024–0247 with ‘‘If no approved
instructions are provided within the
compliance time of paragraph (1) of this AD,
paragraph (2) of this AD must be
accomplished before further flight. The
affected part is eligible to be considered a
serviceable part based on the content of the
Collins Aerospace approved instructions,
once received and accomplished, as required
in paragraph (1) of this AD.’’
(5) This AD does not adopt the ‘‘Remarks’’
section of EASA AD 2024–0247.
(i) Additional AD Provisions
The following provisions also apply to this
AD:
(1) Alternative Methods of Compliance
(AMOCs): The Manager, AIR–520, Continued
Operational Safety Branch, FAA, has the
authority to approve AMOCs for this AD, if
requested using the procedures found in 14
CFR 39.19. In accordance with 14 CFR 39.19,
send your request to your principal inspector
or responsible Flight Standards Office, as
appropriate. If sending information directly
to the manager of the Continued Operational
Safety Branch, send it to the attention of the
person identified in paragraph (j) of this AD
and email to: AMOC@faa.gov. Before using
any approved AMOC, notify your appropriate
principal inspector, or lacking a principal
inspector, the manager of the responsible
Flight Standards Office.
(2) Contacting the Manufacturer: For any
requirement in this AD to obtain instructions
from a manufacturer, the instructions must
be accomplished using a method approved
by the Manager, AIR–520, Continued
Operational Safety Branch, FAA; or EASA; or
Airbus SAS’s EASA Design Organization
Approval (DOA). If approved by the DOA,
the approval must include the DOAauthorized signature.
KHAMMOND on DSK9W7S144PROD with RULES
(j) Additional Information
For more information about this AD,
contact Timothy Dowling, Aviation Safety
Engineer, FAA, 2200 South 216th St., Des
Moines, WA 98198; phone 206–231–3667;
email timothy.p.dowling@faa.gov.
15:42 Feb 10, 2025
Jkt 265001
Issued on February 4, 2025.
Peter A. White,
Deputy Director, Integrated Certificate
Management Division, Aircraft Certification
Service.
[FR Doc. 2025–02494 Filed 2–7–25; 11:15 am]
BILLING CODE 4910–13–P
DEPARTMENT OF HEALTH AND
HUMAN SERVICES
Office of the Secretary
45 CFR Part 162
[CMS–0056–F2]
RIN 0938–AU19
Administrative Simplification:
Modifications of Health Insurance
Portability and Accountability Act of
1996 (HIPAA) National Council for
Prescription Drug Programs (NCPDP)
Retail Pharmacy Standards; and
Modification of the Medicaid Pharmacy
Subrogation Standard; Delay of
Effective Date
Office of the Secretary,
Department of Health and Human
Services (HHS).
ACTION: Final rule; delay of effective
date.
AGENCY:
(k) Material Incorporated by Reference
(1) The Director of the Federal Register
approved the incorporation by reference of
the material listed in this paragraph under 5
U.S.C. 552(a) and 1 CFR part 51.
(2) You must use this material as
applicable to do the actions required by this
AD, unless this AD specifies otherwise.
(i) European Union Aviation Safety Agency
(EASA) AD 2024–0247, dated December 18,
2024.
(ii) Collins Aerospace Vendor Service
Information Letter FA3T1–27–04, dated
August 6, 2024.
(3) For EASA material identified in this
AD, contact EASA, Konrad-Adenauer-Ufer 3,
50668 Cologne, Germany; telephone +49 221
8999 000; email ADs@easa.europa.eu;
website easa.europa.eu. You may find this
material on the EASA website at
ad.easa.europa.eu.
(4) For Collins Aerospace material
identified in this AD, contact Collins
Aerospace, Customer Support Center, 2730
West Tyvola Road, Charlotte, NC 28217;
VerDate Sep<11>2014
telephone 860–654–2500; email
publications@collins.com; website
customers.collinsaerospace.com.
(5) You may view this material at the FAA,
Airworthiness Products Section, Operational
Safety Branch, 2200 South 216th St., Des
Moines, WA. For information on the
availability of this material at the FAA, call
206–231–3195.
(6) You may view this material at the
National Archives and Records
Administration (NARA). For information on
the availability of this material at NARA,
visit www.archives.gov/federal-register/cfr/
ibr-locations or email fr.inspection@nara.gov.
In accordance with the
Presidential memorandum of January
20, 2025, titled ‘‘Regulatory Freeze
Pending Review,’’ the effective date of
the final rule titled ‘‘Administrative
Simplification: Modifications of Health
Insurance Portability and
Accountability Act of 1996 (HIPAA)
National Council for Prescription Drug
Programs (NCPDP) Retail Pharmacy
Standards; and Modification of the
Medicaid Pharmacy Subrogation
Standard’’ is delayed until April 14,
2025. That final rule adopted updated
versions of the retail pharmacy
standards for electronic transactions
adopted under the Administrative
Simplification subtitle of HIPAA, which
constitute modifications to the adopted
standards for the following retail
SUMMARY:
PO 00000
Frm 00007
Fmt 4700
Sfmt 4700
9289
pharmacy transactions: health care
claims or equivalent encounter
information; eligibility for a health plan;
referral certification and authorization;
and coordination of benefits. It also
adopted a modification to the standard
for the Medicaid pharmacy subrogation
transaction.
DATES:
Effective date: The final rule titled
‘‘Administrative Simplification:
Modifications of Health Insurance
Portability and Accountability Act of
1996 (HIPAA) National Council for
Prescription Drug Programs (NCPDP)
Retail Pharmacy Standards; and
Modification of the Medicaid Pharmacy
Subrogation Standard,’’ which appeared
in the December 13, 2024, Federal
Register (89 FR 100763) is delayed to
April 14, 2025. The incorporation by
reference of certain publications
adopted in the rule and approved by the
Director of the Federal Register is also
delayed to April 14, 2025.
Compliance Date: The compliance
dates are extended to April 14, 2028.
FOR FURTHER INFORMATION CONTACT:
Geanelle G. Herring, (410) 786–4466.
Christopher S. Wilson, (410) 786–3178.
SUPPLEMENTARY INFORMATION: Under 5
U.S.C. 553(b) of the Administrative
Procedure Act (APA), the agency is
required to publish a notice of proposed
rulemaking in the Federal Register
before the provisions of a rule take
effect. In addition, section 553(d) of the
APA mandates a 30-day delay in the
effective date after issuance or
publication of a rule. However, to the
extent that 5 U.S.C. 553 applies to this
action, it is exempt from such
requirements because it constitutes a
rule of procedure under 5 U.S.C.
553(b)(A).
Alternatively, HHS’s implementation
of this action without opportunity for
public comment, effective immediately,
is based on the good cause exceptions
in 5 U.S.C. 553(b)(B) and (d)(3). Seeking
public comment is impracticable,
unnecessary, and contrary to the public
interest. The temporary delay in the
effective date until April 14, 2025, is
necessary to give agency officials the
opportunity for further review and
consideration of the new regulation,
consistent with the memorandum
described previously. Given the
imminence of the effective date and the
brief length of the extension of the
effective date, seeking prior public
comment on this temporary delay
would have been impracticable, as well
as contrary to the public interest in the
orderly promulgation and
implementation of regulations. HHS
also believes that affected entities need
E:\FR\FM\11FER1.SGM
11FER1
9290
Federal Register / Vol. 90, No. 27 / Tuesday, February 11, 2025 / Rules and Regulations
KHAMMOND on DSK9W7S144PROD with RULES
to be informed as soon as possible of the
extension and its length in order to plan
and adjust their implementation process
accordingly.
Moreover, we are cognizant that the
final rule that appeared in the December
13, 2024, Federal Register (89 FR
100763) requires publication in the
Federal Register of a correction
document as a technical error was made
in the calculation of the date of the 8month transition period prior to full
compliance with the retail pharmacy
and Medicaid pharmacy subrogation
standards. References in that final rule
VerDate Sep<11>2014
15:42 Feb 10, 2025
Jkt 265001
to August 11, 2027 should, instead, read
June 11, 2027. The delay by virtue of
this final rule will permit more time to
publish those corrections, while also
signaling the nature of those
forthcoming corrections, thereby
minimizing public confusion.
Consistent with the Presidential
memorandum of January 20, 2025,
‘‘Regulatory Freeze Pending Review’’,
we are postponing for 60 days the
effective date of the final rule that
appeared in the December 13, 2024,
Federal Register (89 FR 100763), for the
purpose of reviewing any questions of
PO 00000
Frm 00008
Fmt 4700
Sfmt 9990
fact, law, and policy. As a result,
undertaking notice and comment
procedures for this rule is unnecessary
and contrary to the public interest, and
we find good cause to waive the notice
and comment requirements and the 30day delay in the effective date. Based on
these findings, this rule is effective
immediately upon publication in the
Federal Register.
Dorothy A. Fink,
Acting Secretary, Department of Health and
Human Services.
[FR Doc. 2025–02511 Filed 2–10–25; 8:45 am]
BILLING CODE 4120–01–P
E:\FR\FM\11FER1.SGM
11FER1
Agencies
[Federal Register Volume 90, Number 27 (Tuesday, February 11, 2025)]
[Rules and Regulations]
[Pages 9289-9290]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2025-02511]
=======================================================================
-----------------------------------------------------------------------
DEPARTMENT OF HEALTH AND HUMAN SERVICES
Office of the Secretary
45 CFR Part 162
[CMS-0056-F2]
RIN 0938-AU19
Administrative Simplification: Modifications of Health Insurance
Portability and Accountability Act of 1996 (HIPAA) National Council for
Prescription Drug Programs (NCPDP) Retail Pharmacy Standards; and
Modification of the Medicaid Pharmacy Subrogation Standard; Delay of
Effective Date
AGENCY: Office of the Secretary, Department of Health and Human
Services (HHS).
ACTION: Final rule; delay of effective date.
-----------------------------------------------------------------------
SUMMARY: In accordance with the Presidential memorandum of January 20,
2025, titled ``Regulatory Freeze Pending Review,'' the effective date
of the final rule titled ``Administrative Simplification: Modifications
of Health Insurance Portability and Accountability Act of 1996 (HIPAA)
National Council for Prescription Drug Programs (NCPDP) Retail Pharmacy
Standards; and Modification of the Medicaid Pharmacy Subrogation
Standard'' is delayed until April 14, 2025. That final rule adopted
updated versions of the retail pharmacy standards for electronic
transactions adopted under the Administrative Simplification subtitle
of HIPAA, which constitute modifications to the adopted standards for
the following retail pharmacy transactions: health care claims or
equivalent encounter information; eligibility for a health plan;
referral certification and authorization; and coordination of benefits.
It also adopted a modification to the standard for the Medicaid
pharmacy subrogation transaction.
DATES:
Effective date: The final rule titled ``Administrative
Simplification: Modifications of Health Insurance Portability and
Accountability Act of 1996 (HIPAA) National Council for Prescription
Drug Programs (NCPDP) Retail Pharmacy Standards; and Modification of
the Medicaid Pharmacy Subrogation Standard,'' which appeared in the
December 13, 2024, Federal Register (89 FR 100763) is delayed to April
14, 2025. The incorporation by reference of certain publications
adopted in the rule and approved by the Director of the Federal
Register is also delayed to April 14, 2025.
Compliance Date: The compliance dates are extended to April 14,
2028.
FOR FURTHER INFORMATION CONTACT:
Geanelle G. Herring, (410) 786-4466.
Christopher S. Wilson, (410) 786-3178.
SUPPLEMENTARY INFORMATION: Under 5 U.S.C. 553(b) of the Administrative
Procedure Act (APA), the agency is required to publish a notice of
proposed rulemaking in the Federal Register before the provisions of a
rule take effect. In addition, section 553(d) of the APA mandates a 30-
day delay in the effective date after issuance or publication of a
rule. However, to the extent that 5 U.S.C. 553 applies to this action,
it is exempt from such requirements because it constitutes a rule of
procedure under 5 U.S.C. 553(b)(A).
Alternatively, HHS's implementation of this action without
opportunity for public comment, effective immediately, is based on the
good cause exceptions in 5 U.S.C. 553(b)(B) and (d)(3). Seeking public
comment is impracticable, unnecessary, and contrary to the public
interest. The temporary delay in the effective date until April 14,
2025, is necessary to give agency officials the opportunity for further
review and consideration of the new regulation, consistent with the
memorandum described previously. Given the imminence of the effective
date and the brief length of the extension of the effective date,
seeking prior public comment on this temporary delay would have been
impracticable, as well as contrary to the public interest in the
orderly promulgation and implementation of regulations. HHS also
believes that affected entities need
[[Page 9290]]
to be informed as soon as possible of the extension and its length in
order to plan and adjust their implementation process accordingly.
Moreover, we are cognizant that the final rule that appeared in the
December 13, 2024, Federal Register (89 FR 100763) requires publication
in the Federal Register of a correction document as a technical error
was made in the calculation of the date of the 8-month transition
period prior to full compliance with the retail pharmacy and Medicaid
pharmacy subrogation standards. References in that final rule to August
11, 2027 should, instead, read June 11, 2027. The delay by virtue of
this final rule will permit more time to publish those corrections,
while also signaling the nature of those forthcoming corrections,
thereby minimizing public confusion.
Consistent with the Presidential memorandum of January 20, 2025,
``Regulatory Freeze Pending Review'', we are postponing for 60 days the
effective date of the final rule that appeared in the December 13,
2024, Federal Register (89 FR 100763), for the purpose of reviewing any
questions of fact, law, and policy. As a result, undertaking notice and
comment procedures for this rule is unnecessary and contrary to the
public interest, and we find good cause to waive the notice and comment
requirements and the 30-day delay in the effective date. Based on these
findings, this rule is effective immediately upon publication in the
Federal Register.
Dorothy A. Fink,
Acting Secretary, Department of Health and Human Services.
[FR Doc. 2025-02511 Filed 2-10-25; 8:45 am]
BILLING CODE 4120-01-P