The Regulatory Landscape for Medical Devices at the Close of 2023
With new laws affecting medical devices on the horizon, we discuss changes to the regulatory land...
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With new laws affecting medical devices on the horizon, we discuss changes to the regulatory land...
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European Parliament votes to extend MDR transition periods to avoid supply shortages of medical d...
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Amidst much anticipation, the Medical Devices Regulation becomes fully applicable across the EU f...
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A guide to the classification of devices under the new Medical Devices Regulation
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With the Medical Devices Regulation (MDR) set to become fully applicable next month the European ...
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Artificial Intelligence (AI) is becoming an increasingly pervasive general-purpose technology, wi...
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William Fry are delighted to launch our MDR/IVDR publication. To assist medical device companies ...
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The In Vitro Diagnostic Medical Device Regulation, (EU) 2017/746, is fully applicable as of Thurs...
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The European Commission has announced that it is working on a proposal to postpone the date of ap...
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The Medical Device Coordination Group has published guidance on the activities to be performed by...
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Continuing our series of publications, in this briefing we examine the key changes to the regulat...
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The European Commission proposes a progressive roll-out of the In Vitro Medical Devices Regulatio...
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The European Commission has proposed reclassifying certain beauty and brain stimulation devices w...
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The European Parliament and European Council recently approved the progressive roll-out of the In...
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Charleen O’Keeffe discusses some of the regulatory trends and challenges she sees coming down the...
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In this article, we consider the current status of registration requirements for economic operato...
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Continuing our series of publications, in this briefing we explore which EU Notified Bodies have ...