Adverse Event & Safety Reporting -Clinical Trial Pharmacovigilance

University of Birmingham
Start Date/Time:
16/11/2018 09:30:00

As a result of this course, participants will be able to recognise the importance of pharmacovigilance in clinical trials, be able to recognise different types of adverse events, be aware of legal requirements with regard to reporting adverse eventsand be able to implement local SAE reporting procedures