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GCP-Quality Assurance-Monitoring

Welcome to the "GCP: Quality Assurance/Monitoring" Working Group:

This working group is devoted to all activities referring to quality management in clinical drug research and development. It is also a discussion forum which allows to communicate all GCP related issues. Special attention is directed at national and European regulations for clinical trials. The group particularly deals with the interpretation and implementation of new GCP requirements and comments on its application in clinical drug research. Exchange of information and practical experience is another focal point of this working group.

The group meets regularly every 3 to 4 months.

If you have questions please contact:

Andreas Horstmann
Leiter Qualit├Ątsmanagement
Strathmann GmbH & Co. KG
Sellhopsweg 1
22459 Hamburg
Tel: 0049 40 55905740
Mobil: 0049 151 12558186
eMail: andreas.horstmann@strathmann.de

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