in vitro device

EU Commission Proposes to Extend MDR/IVDR Deadlines

The Commission of the European Union (EU) has proposed extending the transition period for...

The EU’s MDR and IVDR Are Published!

The European Union’s (EU’s) new regulations applicable to medical devices and in vitro diagnostic devices have finally been published.

Digital Sponsors

Become a Sponsor

What's New

Averna Acquires Automated Test Solutions Provider ELCOM

Bureau Veritas Closes Mexico Acquisition

Product Insights: The Most Important Skill to Develop as a Compliance Professional

FDA Proposes Ban on Electrical Stimulation Devices

TDK Releases New Output Voltage Power Supplies for Medical/Industrial Devices

- From Our Sponsors -