The most resource-intensive part of a new drug development is the clinical trial managment and conduct. The protocol defines all aspects of the trial and, in the end, the fate of the drug.
During the webinar, we will study the key factors of successful development of the clinical trial protocol, allowing to observe the appropriate balance between volume and quality of the data received, timeframe and budget of the trial.
What will we discuss in Webinar?
How to choose a clinical trial design
Specifics of the protocol development
For drug developers, pharmaceutical and biotech companies, participants in the clinical trial market, doctors.
Natalia Vostokova, IPHARMA Chief Operating Officer