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HHS/FDA RIN: 0910-AH96 Publication ID: Fall 2020 
Title: Updated Regulations for Medical Gases 
Abstract:

FDA intends to propose revisions to certain regulations with regard to medical gases. These proposed changes are anticipated to include, but are not necessarily limited to, specific changes to current good manufacturing practice (cGMP), labeling, and postmarket reporting regulations applicable to medical gases, generally aiming for less stringent regulation where appropriate.

 
Agency: Department of Health and Human Services(HHS)  Priority: Substantive, Nonsignificant 
RIN Status: Previously published in the Unified Agenda Agenda Stage of Rulemaking: Proposed Rule Stage 
Major: No  Unfunded Mandates: No 
EO 13771 Designation: Regulatory 
CFR Citation: Not Yet Determined     (To search for a specific CFR, visit the Code of Federal Regulations.)
Legal Authority: Pub. L. 115-31, sec. 756 (2017 Consolidated Appropriations Act)   
Legal Deadline:
Action Source Description Date
Final  Statutory  Statute enacted in May 2017 with July 2017 final rule deadline  07/15/2017 

Overall Description of Deadline: Section 756 of the 2017 Consolidated Appropriations Act (Pub. L. 115-31) directs FDA to issue final regulations revising the Federal drug regulations with respect to medical gases by July 2017.

Timetable:
Action Date FR Cite
NPRM  08/00/2021 
Regulatory Flexibility Analysis Required: Undetermined  Government Levels Affected: Undetermined 
Federalism: Undetermined 
Included in the Regulatory Plan: No 
RIN Data Printed in the FR: No 
Agency Contact:
David Faranda
Senior Regulatory Counsel
Department of Health and Human Services
Food and Drug Administration
Center for Drug Evaluation and Research, 10903 New Hampshire Avenue,
Silver Spring, MD 20993
Phone:301 796-8767
Email: david.faranda@fda.hhs.gov