Patient reported outcome endpoints
About
In recent years, various guidelines have been developed to promote the optimal planning, collection, analysis and reporting of PRO endpoints in clinical trials. Join Dr Rebecca Mercieca-Bebber from the NHMRC Clinical Trials Centre for a presentation that will introduce those resources, and provide some top tips for successfully and collaboratively planning and implementing PRO endpoints in a clinical trial.Location
Online event access details will be provided by the event organiser