CGA PS-54

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The U.S. Food and Drug Administration (FDA) drug registration and listing regulations, Title 21 of the U.S. Code of Federal Regulations (21 CFR) Part 207, do not address the unique properties of designated medical gas mixtures. Certain accommodations as presented in this position are made to conform with FDA?s requirements for electronic registration and listing submissions.

Product Details

Edition:

1st

Published:

02/01/2018

Number of Pages:

2

File Size:

1 file , 94 KB