DDF22 – Drug Safety For Medical Writers: Part 1 – Adverse Events and Concomitant Medication

Description

This workshop is designed to give medical writers insight into the processes by which adverse event and concomitant medication data are generated and recorded during clinical trials and the subsequent handling of the data. On completion of the workshop package, participants should be confident in their approach to writing the adverse event and concomitant medication sections of documents relating to clinical trials.

Participant profile: This workshop is intended for people who are new to medical writing and who are involved in writing the safety sections of clinical study reports or related safety summaries.