Introduction to Pharmaceutical Excipients
1:41:22
Determination of Appropriate GMP's for Excipients
1:07:46
Development and Delivery of Pharmaceutical Products (CMC) - MaRS Best Practices
1:01:49
Introduction to Analytical Quality by Design (AQbD) principles
1:02:17
Qualification of Dissolution Testers USP Performance Verification Test (PVT)
47:50
Panel Discussion on Nitrosamines - Past, Present, and Future
1:20:11
Drug Formulation & Delivery with Dr. Robert Ternik
1:03:28
Microbiological Control in a Pharmaceutical Manufacturing Environment
58:50