USP 665 and 1665 Extractables for Components in Pharmaceutical and Biopharmaceutical Manufacturing
38:39
Assisting Companies in the Qualification of Single-Use Materials
46:14
Toxicological Safety Assessment of Process Equipment-Related Leachables in the context of USP (665)
1:32:45
Second Webinar on the architecture of the AI Act
1:29:52
steam sterilization, how it all works
55:57
Discoveries on Applying the New ISO 10993 17
35:50
USP (665) Focus on Component Qualification – What About Component Selection?
1:02:22
AKUS Webinar
29:33