Clinical Research is one of the most regulated industries in the world. Not a surprise, as we are dealing with research involving human beings. Therefore, safeguarding study participant’s rights, wellbeing and safety is of utmost importance. This is why before starting a clinical trial, you need to obtain appropriate approvals. Authorities and Ethics Committees play a major role in this approval process.
This ½-day course is designed to provide basic understanding of the current regulatory requirements for Clinical Trials for people who have limited or no background in these matters.
Chiara Zavattaro
Janssen
The trainer was FANTASTIC. She knew a lot, was extremely friendly, and was open to reply (and she knew the answer to) any question on the topic
Eline Thienpondt
Janssen
The trainer was well prepared, open and friendly - The trainer gave you the chance to ask questions - The system with the voting buttons was very interactive - Interactive session for people who are quite new in the field of regulatory.
Veronique Shiwa