Regulatory Affairs For Clinical Trials

This immersive 2-day training course provides you with all the essential regulatory expertise and updates to run a clinical trial from start to finish and beyond; including market authorisation and pharmacovigilance.

Through a combination of theory, case studies and practical discussion sessions, this course will help you understand current regulations as well as upcoming legislation to be implemented in the clinical trials space.

Master submitting to the clinical trials information system (CTIS). Prepare for regulatory inspection. Deploy good clinical and manufacturing practice. Do all of this and more in the EU, US and internationally.