1:23:57

Cleaning Validation Regulatory Guidelines for the Pharmaceutical Industry

1:27:58

Challenges in Analytical Method Transfer

2:21:51

Qualification and Validation principles to meet revised schedule M requirements

1:43:30

Data Integrity

1:18:50

Statistical Concepts of Process Validation

2:19:43

Revised Schedule M Practical approach to implement Quality Risk Management

1:14:56

HEAL Connections: Designing and Evaluating Health Care Innovations for Downstream Implementability

1:29:16

STERIS Workshop: Important Elements of Cleaning Validation and Health Based Exposure Limits