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 [...]
Innovation and Regulation: How the AI Airlock Sandbox Can Help Medical Device Manufacturers!
Are you a developer or manufacturer of Artificial Intelligence (AI)-based [...]
Global IVD Device Registration: IVDR – 2017/746 Challenges
The IVDR (In Vitro Diagnostic Regulation 2017/746) has drastically changed [...]
Why is now the perfect time to introduce your Medical Devices in Switzerland?
In the current context, Switzerland offers unparalleled opportunities to expand [...]
🚀 See You at MEDICA 2024! 🚀
We’re excited to announce our participation in MEDICA 2024 in [...]
🚨 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 crucial [...]
🌟 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 be [...]
