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Agenda
Free Regulatory Checkup for MedTech
Le 13 mars 2019
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

 

> Inscription HERE<

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