Understanding the Essentials of the Clinical Supply Chain

This intensive session will focus on drug development and what goes into planning for and delivering a study drug for a clinical trial.

Learn the fundamentals of the clinical supply chain via theory and real-life case study examples, setting you up for success in this industry.

Topics will include:
●      Reasons behind Good Manufacturing Practices (cGMPs)
●      Phases of new drug development and approval
●      Randomizing and blinding clinical trial materials
●      Quality assurance and documentation
●      Protocol interpretation
●      Patient compliance
●      Labeling
●      Standard operating procedures (SOPs)
●      Stability
●      Good Distribution Practices (GDPs)
●      Returned drug accountability
●      Changing regulations in the European Union (EU) and rest of world (ROW)