Pharmaceutical Regulation and Registration Procedures in Japan

Sample Size Selection in a Clinical Trial

Data Management for Non-Data Managers

Effective Utilization and Management of Contract Development and Manufacturing Organizations (CDMO’s)

Best Practices for CMC Section Preparation for IND’s and IMPD’s

Fast Track pre-IND CMC Projects

Analyzing Environmental Monitoring Data in Cleanrooms

Foundations of Investigation in Pharma and Medical Device Industries

Medical Device Registration: Strategies to Place your Devices in the EU, UK and US

Introduction to AI-integrated Medical Devices Regulatory Compliance