Agenda for " Content-related and legal challenges in planning and performing clinical trials with medicinal products (in Germany)"

Date: Novembre 10th, 2016
Time: 10:00 – 11:00

The Webinar will be held in German. However, we are happy to answer your questions in English, either during or after the official Webinar. Constanze Stammer, Managing Direktor at PHARMALOG Institute for Clinical Studies “Institut für Klinische Forschung GmbH” in Munich will present the relevant paragraphs of the German Medicines Law (Arzneimittelgesetz) and the GCP-regulation. Furthermore, the different phases of clinical trials during the drug development process and the schedule of a clinical trial will be dealt with.

Moderation and Discussion: Dr. Caroline Schmidt-Lucke, MD, PhD, Assistant Professor Charité, MEDIACC GmbH


10:00 Welcome and introduction PD Dr. Caroline Schmidt-Lucke, MEDIACC GmbH

10:05 Lecture by Constanze Stammer, PHARMALOG Institute for Clinical Research GmbH

10:35 Questions and Discussion

ca. 10:55 End of Webinar

Participation is free of charge. Only telephone costs result.
To participate, please register in advance to info @ or .

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