Your Responsibilities as a Sponsor at a Glance
Webcode 25022110
Alexander Maur
Kanzlei am Ärztehaus Frehse Mack Vogelsang, Cologne (Bayenthal), GERMANY
Lawyer and Partner
More information please click here.
Anja Braschoß
BRASCHOSS-CONSULTING.SOLUTIONS, Gießen, GERMANY
Consultant, Senior Regulatory and Clinical Expert
More information please click here.
Dr. Karen Edelmann-Stergiou
Boehringer Ingelheim Pharma GmbH & Co. KG, Biberach an der Riß, GERMANY
Senior Principal Capability Manager
Dr. Stephanie Blum
cirQum, Frankfurt
General Manager
More information please click here.
24-25/02/2025
24-25/02/2025
both days 09:00 - 12:00 and 13:00 - 16:00 CET
online
online
Veranstaltung - 1,990 € zzgl. MwSt.
The fee includes high-quality course materials (available for download), a certificate of participation, access to our Learning Space and technical support, including a test meeting.
Veranstaltung - 1,990 € zzgl. MwSt.
The fee includes high-quality course materials (available for download), a certificate of participation, access to our Learning Space and technical support, including a test meeting.
Regine Görner
deputy department manager
r.goerner@forum-institut.de
v.kluever@forum-institut.de
Are you looking for a compact knowledge update on the regulations and guidelines in clinical drug trials to perform your daily work in a compliant and responsible manner? Then get comprehensive information in this webcast series!
To undertake a role in clinical drug trials, a comprehensive understanding of compliance, adherence to laws, regulations, and defined requirements is essential.
This 4-part webcast series provides you with a concise two-day knowledge update on all compliance requirements in clinical trials within the European scope.
Starting with the regulations that form the basis for all actions in clinical studies, you will learn about the requirements for patient and drug safety, as well as the responsibilities of sponsors in clinical trials. Data integrity, risk-based quality management, and collaboration with contract partners will also be covered, as will the correct handling of the investigational medicinal product itself.
Equipped with this knowledge, you will be able to carry out your work in clinical trials in Europe independently and in compliance with regulations.
A post-training examination ensures that the knowledge imparted is retained and readily applicable.
24.02.2025 09:00 - 12:00
Alexander Maur
24.02.2025 13:00 - 16:00
Anja Braschoß
25.02.2025 09:00 - 12:00
Dr. Karen Edelmann-Stergiou
25.02.2025 13:00 - 16:00
Dr. Stephanie Blum
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