Medidee is a leading Consultancy Service exclusively supporting Medical Devices and IVD compliance with international regulatory requirements.

A structured team of experts efficiently supplying regulatory and quality expertise along the entire product lifecycle, from idea to market, from market to profitability.

Our services include:

– Regulatory & Clinical Pathway Development
– Implementation of Quality Management Systems
– Internal Audit programs
– Technical documentation – Submissions
– Clinical evaluation
– Risk Management – EN ISO 14971
– Verification and Validation (V&V)
– Marketing & Post Marketing
– Supplier controls


Learn more about Medidee, visit their website

Pierre Geens, Senior Consultant
+32 473 64 20 53

Any questions about Medidee? Meet the team on March 22, 2018 in the exhibition area !