Conference Date: 10 Jul 2009
Conference Ref: A7-4309
Fee: £545 + VAT
Venue: The Rembrandt Hotel, London
This comprehensive seminar will cover :-
- The current regulatory situation for safety reporting in the EU
- Ethics and Investigators
- Determining the best approaches from CIOMS for clinical trials
- Understand how best to present safety data in the Investigator Brochures
- The role of the developmental safety update report (as recommended by CIOMS)
You will also discuss what Regulators want to see from GCP Inspections in terms of processes (SOPs) and training and what are the most common findings presented from Inspections.
Click here to register for this important event