How Accurate Adverse Event Reporting is the Key to Subject Safety of Approved Drugs 2018
06 Feb 2018
Webinar
Description
Topics
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
Who should Attend
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
Past Events
How Accurate Adverse Event Reporting is the Key to Subject Safety of Approved Drugs 2018 - 06 Feb 2018, Webinar (72918)
Important
Please, check "How Accurate Adverse Event Reporting is the Key to Subject Safety of Approved Drugs" official website for possible changes, before making any traveling arrangements
