CGA M-2
CGA M-2
General Guide for the Manufacturer of Medical Gases Classified as Drugs
Handbook / Manual / Guide published 01/01/2013 by Compressed Gas Association
Categories
- ASME BPVC 2019
- ANSI
- ASME
- ASME BPVC
- API
- ASTM
- SAE
- BS
- 2019
- 2020
- 9000
- AASHTO
- AATCC
- ABMA
- ACC
- ACI
- ARINC
- AS
- ASA
- ASD-STAN
- ASQ
- AWS
- AWWA
- B11
- BHMA
- CAN/CGSB
- CAN/ULC
- CECC
- CGA
- CIE
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- EURO
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- IEC
- IEEE
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- ISO
- JIS
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- NCSL
- NETA
- New Standards
- NSF
- PIP
- RICA
- RTCA DO
- SMACNA
- TIA
- TMS
- USP
- UTS
- VDI
Full Description
This publication applies to firms that engage in the filling, repackaging, transfilling, mixing, and/or re-labeling of compressed medical gases (CMG) classified as drugs by the FDA and applicable state agencies. Although it is primarily intended for firms engaged in the CMG manufacturing processes, portions may apply to firms that only distribute CMG classified as drugs.Cart
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