Potential Designs for Leachable Studies on Biopharmaceutical Manufacturing Equipment
29:33
Good Identification Practices in Non-Targeted Screening Analyses
53:05
USP 665 and 1665 Extractables for Components in Pharmaceutical and Biopharmaceutical Manufacturing
25:38
Qualification of Single Use Materials for Biopharmaceutical Manufacturing
46:14
Toxicological Safety Assessment of Process Equipment-Related Leachables in the context of USP (665)
38:39
Assisting Companies in the Qualification of Single-Use Materials
20:43
Simon Sinek's Advice Will Leave You SPEECHLESS 2.0 (MUST WATCH)
57:41
At-Line Monitoring Coupled With DOE for Higher IVT Yield and Efficiency of Purification
1:00:46