EUDAMED Registration – A Comprehensive Guide for Manufacturers
EUDAMED registration is an important part of placing and [...]
Team-NB Guide December 2024: Your Complete Resource for Medical Device Certification
On December 18th, 2024, Team-NB, the European Association of [...]
Arab Health 2025: Join Us in Dubai!
We’re excited to announce our participation in Arab Health 2025, [...]
Public Consultation on the Evaluation of EU Regulations for Medical Devices and In Vitro Diagnostics: Have Your Say!
The European Commission has initiated a public consultation to assess [...]
Important Update on Medical Device Regulation in the UK
The UK government has outlined a roadmap for a [...]
Master UDI-DI for Contact Lenses: What Manufacturers Need to Know
Learn about the new Master UDI-DI for contact lenses: [...]
Streamline Your Compliance Process with the New CAPA Template – MDCG 2024-12
The MDCG 2024-12 template is a vital tool for managing [...]
Eudamed modules: Key steps for medical device compliance
What is Eudamed and why is it important? Eudamed is [...]
Post-Market Surveillance (PMS): A Key Pillar for Compliance and Innovation in the Medical Device Industry
In the rapidly evolving field of medical devices, compliance with [...]
Is the FSC valid indefinitely, or does it have an expiration date?
If you’re a medical device manufacturer, understanding the validity [...]
