Last Friday, we had the privilege of hosting the meeting for three working groups of the German Quality Management Association e.V. (GQMA). We were delighted to welcome the GCP Quality Management, Medical Devices, and Analytics groups.
After a short introduction to our company by Beate Hientzsch and Bernd Hientzsch, we were honored to hear from our main speaker, Tobias Bartl, Regulatory Affairs Expert at CE plus. Tobias delivered two compelling presentations on the In Vitro Diagnostic Regulation (IVDR), providing valuable insights into this critical area.
Following a productive lunch break filled with networking opportunities, the afternoon session covered updates on clinical studies related to medical devices, along with the GQMA’s review and comments on ICH-GCP R3.
We truly appreciated the lively and cooperative atmosphere of the meeting, which encouraged a dynamic exchange of ideas. A big thank you to everyone who attended and contributed to this event.
Posted on LinkedIn by Katrin Besch