Standard Operating Procedures of the Research Ethics Committee

26 February 2003
print version

Objective: To ensure that the content of the clinical trial documentation is relevant and accurate, the submissions are prepared and progressed in a consistent manner, and are subject to appropriate ethical review and approval procedures.

Learn More To give you the best possible experience, our sites use cookies. Continuing with cookies enabled means you're OK with this. Click Learn More for more information about our cookies, and how to disable them. ×