What is the IFU and why is it crucial for medical devices?
When it comes to medical devices, ensuring safety, compliance, [...]
Discover how to register your medical devices in Europe: an essential guide for manufacturers outside the EU!
Are you a manufacturer outside the EU and wondering how [...]
Clinical Research in Medical Devices: What Role Does the Manufacturer Play?
Clinical research is fundamental to ensuring the safety and effectiveness [...]
Exciting news! We’re heading to CMEF, the International Medical Device Fair in Shenzhen!
Join us from October 12 to 15, 2024, at [...]
Importers or Distributors: Who is Responsible for Medical Device Compliance?
Understanding the responsibilities of importers and distributors is fundamental [...]
Discover the 6 Steps to Successfully Obtain CE Certification
If you’re developing a medical or in vitro diagnostic device, [...]
Exciting Update: Istituto Superiore di Sanità Now Accredited for IVDR!
A new key player has been designated for the [...]
CMC MEDICAL DEVICES & DRUGS, S.L. Obtains ISO 13485:2016/A11:2021 Certification, Reaffirming Its Commitment to Quality and Safety in the Medical Industry
CMC MEDICAL DEVICES & DRUGS, S.L., a company dedicated [...]
New Artificial Intelligence Law Comes Into Force Today, August 1, 2024: Key Points and Focus on High-Risk Devices
The European Parliament and the Council of the European Union [...]
Key Updates in Regulation (EU) 2024/1860: Implications for the Medical Device Industry
The new regulation brings significant changes that will impact [...]
