Adverse Event & Safety Reporting – Clinical Trial Pharmacovigilance

Venue:
NIHR/Wellcome Trust Birmingham CRF, Birmingham
Start Date/Time:
04/11/2020 09:30:00
Summary

Attendees 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 events and be able to implement local SAE reporting procedures