- October 6, 2021
- By: Marc Chaillou
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.
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The EU Medical Device Regulations (MDR) states any device manufacturer with a website must publish user information in electronic form.
Over the last few posts, we have been touching upon different labelling requirements set by the MDR.
The new European Database on Medical Devices, known as EUDAMED, was originally scheduled to launch in May 2020,
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