Adverse Event & Safety Reporting -Clinical Trial Pharmacovigilance

Venue:
NIHR/Wellcome Trust Birmingham CRF, Birmingham
Start Date/Time:
13/11/2017 09:30:00
Summary

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