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CGA/GAS - CGA M-7

STANDARD FOR QUALIFYING SUPPLIERS USED BY MEDICAL GAS MANUFACTURERS, EQUIPMENT MANUFACTURERS, AND DISTRIBUTORS

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Organization: CGA/GAS
Publication Date: 1 January 2017
Status: active
Page Count: 30

Document History

M-7
January 1, 2022
STANDARD FOR QUALIFYING SUPPLIERS USED BY MEDICAL GAS MANUFACTURERS, EQUIPMENT MANUFACTURERS, AND DISTRIBUTORS
This publication applies to medical gas manufacturers, medical gas equipment manufactures, and distributors developing company-specific standard operating procedures (SOP) for qualifying suppliers...
CGA M-7
January 1, 2017
STANDARD FOR QUALIFYING SUPPLIERS USED BY MEDICAL GAS MANUFACTURERS, EQUIPMENT MANUFACTURERS, AND DISTRIBUTORS
A description is not available for this item.
M-7
January 1, 2014
GUIDELINE FOR QUALIFYING SUPPLIERS USED BY MEDICAL GAS MANUFACTURERS AND DISTRIBUTORS
A description is not available for this item.
M-7
January 1, 2009
GUIDELINE FOR QUALIFYING SUPPLIERS USED BY MEDICAL GAS MANUFACTURERS AND DISTRIBUTORS
A description is not available for this item.
M-7
January 1, 2007
GUIDELINE FOR QUALIFYING SUPPLIERS USED BY MEDICAL GAS MANUFACTURERS AND DISTRIBUTORS
A description is not available for this item.
M-7
February 2, 2005
Guidelines for Qualification of Medical Gas Suppliers
A description is not available for this item.
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References

This document is referenced by:
CGA M-1 - STANDARD FOR MEDICAL GAS SUPPLY SYSTEMS AT HEALTH CARE FACILITIES
Published by CGA/GAS on January 1, 2018
A description is not available for this item.
This document is referenced by:
CGA M-5 - GUIDE FOR HOME RESPIRATORY CARE FIRMS FILLING OR DISTRIBUTING LIQUID OXYGEN USP
Published by CGA/GAS on January 1, 2013
This publication is intended to address operations typical to an HRC firm and is not all inclusive. It is primarily intended for firms engaged in the filling (manufacture) and distribution of liquid...
This document is referenced by:
CGA M-11 - GUIDELINE FOR COMPLIANCE WITH THE QUALITY SYSTEMS APPROACH TO CURRENT GOOD MANUFACTURING PRACTICES
Published by CGA/GAS on January 1, 2021
This publication provides guidance on how a medical gas, device gases, and device manufacturers can implement the quality systems approach to meet requirements of 21 CFR Parts 210, 211, and 820 [1].
This document is referenced by:
M-3 - STANDARD FOR THE MANUFACTURER OF BULK MEDICAL GASES
Published by CGA on January 1, 2021
This publication applies to the bulk manufacturing of medical gases as follows: • bulk air separation (oxygen, USP and nitrogen, NF) manufacturing and distribution facilities; • bulk carbon dioxide,...
This document is referenced by:
CGA M-16 - GUIDANCE FOR ELECTRONIC RECORDS & SIGNATURES IN THE U.S. & CANADIAN FOOD, DRUG, & MEDICAL DEVICE GAS & GAS EQUIPMENT INDUSTRY
Published by CGA/GAS on January 1, 2016
A description is not available for this item.
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