This two-day course offers an overview of the drug development process including the following topics:
● Good Clinical Practice / ICH Guidelines / Directives
● “Who’s Who” in clinical research – roles and responsibilities
● Conducting clinical trials: pre-, during and post study activities
● Clinical trial methodology and design
● Understanding and handling of adverse events
● Monitoring clinical studies
Member companies of the Swiss Biotech Association will benefit from a 15 % discount on the registration fee.