Possess ability to differentiate federal regulations versus industry standard practice
Discover process improvements
Ability to determine when an adverse event is an unanticipated problem
Who should Attend
Attendees from:
Research Nurses/ Staff
Principal Investigators
Project Managers
Pharmaceutical Sponsors
Clinical Research Associates
Project Assistants
IRB Staff and Committee Members
Past Events
IRB reporting: Protocol deviations, adverse events, IND safety reports 2017 - 11 Jan 2017, Webinar (64207)
Important
Please, check "IRB reporting: Protocol deviations, adverse events, IND safety reports" official website for possible changes, before making any traveling arrangements
