No matter what your question is, we are experts in the broad field of Regulatory compliance: Our Team of more than 50 Experts knows Technical Documentation, Quality Management, Clinical Affairs, Regulatory Affairs and Medical Device Software as well as Verification and Validation inside out.Your specialists at Metecon - all engineers and scientists - have in-depth clinical and regulatory know-how, experience in mechanics, electronics and software, as well as comprehensive project management skills. We help you to smooth the way for your Medical Devices or IVD. And you can always get the best project team which fulfill your needs and achieve the goal.How can we support you?
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Your Contact Persons at Metecon
Fabiola Hartung-Linz
Director Business Development
M +49 173 3296833
fabiola.hartung-linz@metecon.de
Dunja Schildge-Reichmann
Head of Regulatory Affairs & Quality Management
dunja.schildge-reichmann@metecon.de
Thorsten Stumpf
Project Lead Regulatory Affairs, Software & AI | RAC Devices
thorsten.stumpf@metecon.de
