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MDR

October 6, 2021

Schlafender Hase Team

MDR e-Labeling

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

October 6, 2021

Schlafender Hase Team

MDR Graphic Symbols

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

September 22, 2021

Schlafender Hase Team

MDR UDI and Device Registration

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