After this course, you will have a deep understanding of:
- The Sponsor's responsibilities in Clinical Trials
- How to start building quality into the design of the trials
- How to identify critical-to-quality factors
- The differences in E6 R2 and R3 (according to the draft version)
- ICH E8(R1)
When?
April 18th - 8:30-17:00 hrs (Full-day training)
Where?
Hummeltoftevej 49, 2830 Virum, blok A. The conference department by the canteen. It is at the start of the building, down the ramp and to the left.
Price model
If there are 5 or more people joining from the same organization, we provide a special price. Please contact beatrice.ostrom@pharmarelations.se directly by sending an email.