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]


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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
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