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EU MDR

Our editor Laura Hughes highlights her five must-read articles for this week. Read more

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As the deadline for European Medical Device Regulation (EU MDR) is rapidly approaching, our editor Laura Hughes provides a brief summary of the regulation and shares the results of MPN’s recent survey. Read more

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Sophie Laurenson, medical device consultant at Kolabtree, an online platform for scientists, outlines the major changes in EU MDR and the consequences of these changes. Read more

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The Irish Medtech Association announces its priorities for the next government ahead of the country’s general election on 8th February. Read more

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As regulatory changes, public demand and pure economics drive more labelling content online, what are the considerations for managing all of this? Kallik’s Graham Francis offers some best-practice advice. Read more

Opinion

Our editor Laura Hughes highlights her five must-read articles for this week. Read more

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Our editor Laura Hughes highlights her five must-read articles for this week. Read more

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Despite the impending implementation date in May 2020, many companies have not yet grasped the full impact the new EU Medical Device Regulations (MDR) will have on product labelling. Read more

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Our editor Laura Hughes highlights her five must-read articles for this week. Read more

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Further delays for class I medical devices have been announced following the Council of the European Union’s second corrigendum. Read more

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MedTech Europe has said it remains held back by “slow and piecemeal implementation” of the new In Vitro Diagnostic Medical Device Regulation (IVDR) and Medical Device Regulation (MDR) framework. Read more

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Jalal Bouhdada, founder and CEO for Applied Risk, provides eight steps for strong cybersecurity. Read more

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Trelleborg’s healthcare and medical operation is offering support to its customers in meeting the new EU MDR regulation which comes into force in Member States in May 2020. Read more

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Our editor Laura Hughes highlights her five must-read articles for this week. Read more

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Jon Speer, founder and VP of QA/RA for software company Greenlight Guru, explains the major regulatory changes which are coming soon for manufacturers of medical devices. Read more

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Our editor Laura Hughes highlights her five must-read articles for this week. Read more

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Our editor Laura Hughes provides a brief summary of EU Medical Device Regulation (EU MDR), class I medical devices and the potential delays to EU MDR for class I medical devices. Read more

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Our editor Laura Hughes highlights her five must-read articles for this week. Read more

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Sandi Schaible and Sherry Parker from WuXi Medical Device Testing, talk through what manufacturers need to know about the EU Medical Device Regulation (MDR). Read more

, North America

Medical technology manufacturer, Raumedic, explains how the company is preparing for the enforcement of EU Medical Device Regulations (MDRs). Read more

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