The world's leading automated proofreading software

MDR

2 minutes read

MDR e-Labeling

The EU Medical Device Regulations (MDR) states any device manufacturer with a website must publish user information in electronic form.

2 minutes read

MDR Graphic Symbols

Over the last few posts, we have been touching upon different labelling requirements set by the MDR.

2 minutes read

MDR UDI and Device Registration

The new European Database on Medical Devices, known as EUDAMED, was originally scheduled to launch in May 2020,