🚨 Countdown for MDR Certification: Imminent Deadline for Legacy Devices!
If your medical device is not yet fully compliant [...]
🌟 Why Our MDR Consulting Services Are Essential in the Rehabilitation and Care Sector 🌟
Compliance with the Medical Devices Regulation (MDR 2017/745) is [...]
🌟 We are excited to announce our participation in «Rehacare», The International Trade Fair for Rehabilitation and Care! 🌟
📅 From September 25th to 28th, 2024, we will [...]
🚀 Need to Register in EUDAMED? Here’s How to Get Started! 🚀
If you're a manufacturer, importer, or authorized representative in [...]
🌍 Looking to expand your business globally with medical devices or IVD products? 🚀 Here’s what you need to know about the Free Sale Certificate (FSC)
A Free Sale Certificate (FSC) is a crucial document [...]
Regulatory Alignment Between the EU and Switzerland in In Vitro Diagnostic Medical Devices
On August 14, 2024, Swissmedic, Switzerland's regulatory authority for [...]
August 6th, Swissmedic is rolling out key changes for registration and modification in the CHRN
🔗 New Process: All registration applications and modifications must [...]
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 [...]
New Registration Process for Economic Operators in Switzerland: Key Dates You Can’t Miss!
Exciting news for all manufacturers, authorized representatives, and importers [...]
