Medidee the leading medical and in-vitro diagnostics devices consultancy firm is delighted to invite you to this exclusive opportunity dedicated to MedTech companies.
Benefit of a 1-hour face-to-face open discussion with experts to address your topics such as:
The impact of new European regulations (MDR & IVDR) on your strategy
New product classification and its impacts (medical software, IVD, etc…)
Clinical Evaluation according to MEDDEV 2.7/1 rev 4 and MDR/IVDR
PMS/PSUR
Supply chain management (MAIDS)
Requirements for quality management system according to ISO 13485:2016
….
Location: WSL-CEI1 Louvain-La-Neuve
Chemin du Cyclotron 6
1358 Louvain-La-Neuve
