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About This Item

 

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.
 

Document History

  1. CGA M-2


    Standard for the Manufacture of Medical Gases Classified as Drugs

    • Most Recent
  2. CGA M-2

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    viewing


    General Guide for the Manufacturer of Medical Gases Classified as Drugs

    • Historical Version
  3. CGA M-2


    General Guide for the Manufacturer of Medical Gases Classified as Drugs

    • Historical Version