Clinical trial documents: Joining the dots
Tuesday 14th September 2010
Park Inn, Heathrow, London
This one-day conference will focus on the interface between medical writers and clinical operations professionals. Last year's meeting covered protocol development, and this year's will cover the many further documents used in a clinical trial, from the Investigator Brochure, through regulatory/ethics applications and patient information, to the Case Report Form and the clinical study report. Expert speakers will highlight key pitfalls, share tips on producing effective and practical documents, and encourage clinical personnel and medical writers to collaborate earlier and more deeply.
This will be ICR's third joint symposium with the European Medical Writers Association (EMWA).
Last year's ICR/EMWA joint symposium
Last year's joint symposium
The 2009 ICR/EMWA joint symposium the potential for more effective protocols through greater interaction between clinical operations professionals and medical writers. We have short interviews with Wendy Kingdom RICR and Adam Jacobs FICR CSci, who each chaired sessions at that meeting.
Programme
* Overview of documents & processes - speaker approached
* Case study: Getting it all wrong - Adam Jacobs FICR CSci, Dianthus Medical Ltd
* Investigator brochure - Barry Drees, Trilogy Writing & Consulting
* Patient information - Wendy Kingdom RICR, Wendy Kingdom Ltd
Conferences 
