CGA M-2

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This publication is a standard for compliance with the applicable regulations of the U.S. Food and Drug Administration (FDA) for the manufacture of compressed medical gases (CMG) classified as drugs as described in Title 21 of the U.S. Code of Federal Regulations (21 CFR). It outlines the requirements for manufacturing CMGs classified as drugs; however it may not contain all information necessary to comply with FDA regulations. It is the responsibility of each CMG manufacturer to ensure that their standard operating procedures (SOP) comply with all applicable federal, state, and local regulations.

This publication applies to firms that engage in the filling, repackaging, transfilling, mixing, and/or re-labeling of 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.

Product Details

Edition:

3rd

Published:

01/01/2021

Number of Pages:

48

File Size:

1 file , 530 KB

CGA M-2

• by admin
• Comments Off on CGA M-2
• CGA

Click here to purchase
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.

Product Details

Edition:

2nd

Published:

01/01/2013

Number of Pages:

44

File Size:

1 file , 500 KB