One live webcast per month with proven experts from medical affairs with the possibility of discussion via audio and chat. Rupert Lang, GKM Gesellschaft für Therapieforschung mbH, Chief Operations Officer, gives a lecture on application monitoring (study synopsis, notification, ethical vote, etc.)

Medical devices have to be safe and efficient. Appropriate clinical data are required to substantiate this. Dr. Andrea Röthler gives a lecture in an online event on the subject of clinical trials with medical devices: PMCF studies, planned date April / May 2022

In German language: Seit dem 31.01.2022 ist die Clinical Trial Regulation 536/2014 (CTR) in der Praxis anwendbar. Es gibt eine Übergangsfrist von drei Jahren, in der sowohl die EU Richtlinie 2001/20 als auch die EU Verordnung 536/2014 parallel laufen.

As a full service CRO offering services throughout the entire clinical development, we understand the critical role of EDC in ensuring the success of clinical studies and are committed to providing the most efficient and high-quality solutions. With this in mind, we have organised a webinar together with one of our EDC suppliers, our longstanding partner Clincase, for you to find out about the latest developments in EDC systems for clinical research. We look forward to your registration!