Achieve compliance
for your Medical Device in Europe.

Since the enforcements of the regulations regarding Medical Devices, your Business needs a solid roadmap to access the European market or maintain business continuity.

Scan through the most relevant informations easily with our free guide.

• MDD certificate renewal
• Clean Evaluation Plan and Report (CEP and CER)
• Implementing UDI (Unique Device Identification)
• PRRC (Person Responsible for Regulatory Compliance)
• Post-market Surveillance and Post-market Clinical Follow Up
• Technical File assessment
• Notions about EUDAMED