LOI JARDE

Latest DeviceMed publication LOI JARDE – By Amélie Archer & Lucile Bernard – MedPass International Link below AFCROs2-Loi-Jarde?

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New EU rules on medical devices

New EU rules on medical devices to enhance patient safety and modernise public health The Commission welcomes the adoption of its proposal for two Regulations on medical devices which establish a ...

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EU Clinical Data Requirements Coming With New Regulations

Medtec Insight – Pharma Intelligence I Informa By Sarah Sorrel More EU Clinical Data Requirements Coming With New Regulations IN THE EU, A TWO-STEP STRENGTHENING of requirements for clinical data ...

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The Future Of Clinical Evidence Requirements For CE Marking

The Council of the EU’s agreed amendments to the requirements for clinical evaluation reports under the new Medical Device Regulation are substantial. And so are its proposed amendments to ...

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