Since the development of the ICH GCP guidelines, clinical trials are more and more complex in a stringent regulatory framework. The process of conducting a clinical data is a costing step and the number of wasted dollars is staggering. Setting up and conducting a clinical trial is not easy and sponsors can fall into the trap of the facility and waste a lot of time and money before putting their product on the market. Every clinical trial is actually a project and as any projects, there are hurdles to overcome and best practices to put in place.
Key learning objectives:
- Understand the pitfalls that can be easily be avoided
- How to put in place tools and best practices to ensure a smooth conduct of a clinical trial
- Key take-home message to keep in mind when conducting a clinical trial