Investigator Training
Guidelines for conducting clinical trials with
particular reference to ICH/GCP
Contents:
• Introduction to clinical research
• Guidelines
• Clinical trials and the German Medicines Act (AMG)
• Responsibilities (ICH-GCP)
• Study protocol / Patient information
• Site selection
• Approval procedure
• Site initiation
• Monitoring visits
• Clinical trial logistics
Aim:
In just 1 day this course provides you with the knowledge you need to work as an investigator. Special emphasis is placed on meeting the requirements of the Ethics Committee and conducting clinical trials ICH-GCP quality standards and in accordance with the German Medicines Act.
Dates:
13.08.2010
17.09.2010
15.10.2010
19.11.2010
Venue: PAREXEL-Akademie, Berlin
Cost: € 400,- + VAT
Download registration form (available in German)
Download flyer (available in German)
Download terms and conditions (available in German)