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European Parliament

A new law adopted by the European Parliament on Wednesday, 3rd October, aims to avoid duplicating national health technology assessments to determine a medicine’s added value that helps EU countries decide on pricing. Read more

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European Parliament

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The medtech sector has welcomed the vote from the European Parliament to endorse new regulations on in vitro diagnostic medical devices (IVDR) and the new Regulation on Medical Devices (MDR). Read more

Opinion

EU agrees to tougher rules on authorisation and surveillance of medical devices and in vitro medical devices Read more

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Industry body, MedTech Europe, believe the new adopted healthcare report released by the European Parliament still avoids calls for improved monitoring of patient safety at a national level. Read more

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