MHRA updates Post-Market Surveillance: How to adapt your medical devices to new requirements
The Medicines and Healthcare products Regulatory Agency (MHRA) has released [...]
How to Ensure the Safety of Mobility Devices with Lithium Batteries: MHRA Recommendations
Lithium batteries are a critical technology for powering mobility [...]
IvDO Update 2025: Key Changes in Swiss In Vitro Diagnostic Regulations
As of January 1, 2025, the amended Swiss Ordinance [...]
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 [...]
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 [...]
