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.