On May 6-8, regulatory affairs professionals will gather in Berlin to attend RAPS Euro Convergence 2024. Welcome you to visit our booth and discuss the topical questions around medical device and IVD device regulation!
The Regulatory Affairs Professionals Society (RAPS) event is a great opportunity to build professional knowledge, which is very important for us. Companies in MD, IVD and pharmaceuticals need to respond to constant change and developments in regulatory environment and technologies.
At our booth, you can see some exciting examples of medical devices showcasing the variety we work with and the regulatory challenges that we help the MD and IVD device manufacturers to tackle.
Visit the Labquality booth (TB1 on entry level) to meet with our team of experts: Clinical Research Manager Kirsten Sander; Quality & Regulatory Affairs Manager Terhi Heikkinen; Senior Specialist, QARA Nina Vartiainen and Sales Director Meeri Säily are looking forward to discuss with you.
Contact us
Kirsten Sander
Managing Director, Artimed
kirsten.sander@labquality.com
Meeri Säily
Sales Director, Consulting and Clinical Trials
meeri.saily@labquality.com
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