How Accurate Adverse Event Reporting is the Key to Subject Safety of Approved Drugs 2018 is a webinar that covers topics such as:
- How to know what an Adverse Event is and when to report it or them
- The definitions of Adverse Events, Serious Adverse Events, Unanticipated Adverse Device Effects and many more
- Understanding laboratory AEs and the "Reference Range" concept
- Knowing the AE types and likelihood of finding "rare" events
- Reporting of Adverse Events - when and to whom and the use of AE Terminology systems
- Common Mistakes in AE / SAE Reporting
- How to record Adverse Events and assess causality - the algorithm
How Accurate Adverse Event Reporting is the Key to Subject Safety of Approved Drugs 2018 is intended for:
- Clinical Research Scientists
- Principal Investigators and Sub Investigators
- Clinical Research Associates (CRAs) and Coordinators (CRCs)
- Safety Nurses
- Clinical Research Data Managers
- QA / QC Auditors and Staff