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EU MDR

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

News

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

News

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

News

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

News

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

News

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

News

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

News

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

News

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

News

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

News

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

News

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

News

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

News

Lee Stacey, product evangelist, Thingstream, writes about challenges faced by the medical device industry amidst the growth of IoT, and new European regulations that come into force next year. Read more

Opinion

The editors of Medical Plastics News and Med-Tech Innovation News want to know if you are ready for the enforcement of these regulations. Read more

News

The government state that the MDR will come in to effect in May 2020, and the IVDR in May 2022, however the United States has called upon the EU to delay the implementation of Medical Device Regulations and In Vitro Diagnostic Regulations by 3 years. Read more

News

Sumitomo (SHI) Demag, has pioneered a fully automated in mould decorating production cell. This cell can be used to issue medical devices with unique device identifications ahead of the enforcement of the EU medical device regulations. Read more

North America

Vicki Anastasi, and Karen Hill, ICON, examine the key challenges associated with the new EU MDR and IVDR Read more

Opinion