NSF 363 : 2016
Superseded
View Superseded by
GOOD MANUFACTURING PRACTICES (GMP) FOR PHARMACEUTICAL EXCIPIENTS
English
01-01-2016
03-30-2020
1 General
2 Reference documents
3 Definitions
4 Quality management system
5 Management responsibility
6 Resource management
7 Excipient realization
8 Measurement, analysis and improvement
Gives a comprehensive basis for the quality management system used in the manufacture of pharmaceutical excipients.
| DocumentType |
Standard
|
| Pages |
42
|
| PublisherName |
NSF International
|
| Status |
Superseded
|
| SupersededBy | |
| Supersedes |
| ISO 9001:2015 | Quality management systems — Requirements |
Please Login or Create an Account so you can add users to your Multi user PDF Later.
Important note : All end users must be registered with an Account prior to user licenses being assigned.
Users cannot be edited or removed once added to your Multi user PDF.