The IRB reporting: Protocol deviations, adverse events, IND safety reports 2017 is a webinar that covers topics such as:
- Acquire knowledge regarding reporting requirements
- Possess ability to differentiate federal regulations versus industry standard practice
- Discover process improvements
- Ability to determine when an adverse event is an unanticipated problem
The IRB reporting: Protocol deviations, adverse events, IND safety reports 2017 is intended for attendees from:
- Research Nurses/ Staff
- Principal Investigators
- Project Managers
- Pharmaceutical Sponsors
- Clinical Research Associates
- Project Assistants
- IRB Staff and Committee Members
