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medical devices

Manufacturer, Tessy Plastics, has announced the expansion of warehouse space in one of its manufacturing facilities in Upstate New York. Read more

North America

Revisions have been made by the International Organisation for Standardization (ISO) to its ISO 14971 regulation. Read more

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Medical device manufacturers should ensure their packaging solutions exceed mandatory EU legislation to safeguard quality standards and maintain a contaminant-free environment, according to packaging machinery supplier ULMA. 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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According to GlobalData's deals database, there was a rise of 12.7% in overall deal activity for Europe's medical devices during Q3 of 2019, compared to the four-quarter average. Read more

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India's central government has announced plans to bring all medical devices under the definition of drugs in order to regulate its manufacture and trade. Read more

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A recent report suggests there is room for improvement for quality management systems for medical device manufacturers. Read more

North America

The finding was suggested within a research report from Owen Mumford Pharmaceutical Services which estimates opportunities for emerging biosimilar markets. Read more

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Medical Design & Manufacturing (MD&M) West Conference is returning for its 35th year to the Anaheim Convention Center in Anaheim, CA from February 11 - 13, 2020 for three days of education aimed to inspire the industry. Read more

North America

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Credit: CENTIMFE

Rui Soares, CENTIMFE - technological center for the moldmaking, special tooling and plastic industries from Engineering & Tooling Cluster in Portugal, presents a case study on advanced technological approaches for the development of medical devices. Read more

North America

Stephanie Steichen, technical service and development specialist, DuPont explains the challenges associated with medical wearable technologies. Read more

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The Medical Device Innovation Consortium (MDIC) has been awarded $2.8 million in funding by the U.S. Food and Drug Administration (FDA) for the expansion of the Case for Quality and medical device cybersecurity programs. Read more

North America

Over 2,400 medical device manufacturers from around the world have signed up to use the Global Medical Device Nomenclature (GMDN), the de facto global standard for identifying the world’s medical devices, since April 2019. Read more

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The UK will be leaving the EU on 31 October. This will bring important changes to doing business. Here are six things life science companies can do now to get ready. Read more

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Cybersecurity solutions provider Nova Leah has achieved certification for quality management and information security management. Read more

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NHS Tayside says Datalogic laser marking technology has been an ‘essential asset’ to track and trace reusable medical devices and ensure the prevention of high-risk instrument migration at its Central Decontamination Unit (CDU). Read more

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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

Using design teams in both the UK and China, Industrial Design Consultancy (IDC), has developed the G3 sleep apnoea device for Chinese medical company, BMC. Read more

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The MHRA has reiterated guidance on how medical devices will be regulated in the event of a no deal Brexit. Read more

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Care providers are more susceptible to cyberattacks than ever, according to new research from digital platform security firm Irdeto. Read more

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