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 [...]
Important Notice for Companies with Medical Devices in the European Market.
Attention to all companies with products regulated under Directive [...]
The First Module of the swissdamed Medical Devices Database Launches Online in August
Swissdamed: The New Medical Devices Database in SwitzerlandWe are pleased [...]
CMC Consulting Group celebrates tenth anniversary of CMC Medical Devices with a new corporate image
CMC Consulting Group, a leading holding company in regulatory [...]
NEW Notified Bodies obtained the MDR audit qualification
Two new authorizations have been added to the EU MDR, [...]
