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By Hilde Viroux and Chris Illman, PA Consulting | The EU Commission had issued an extension to manufacturers to sign up with a notified body for EU Medical Devices Regulation (MDR) compliance, but instead, manufacturers have slowed down activities. |
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By Hilde Viroux, PA Consulting | The EU AI Act is a landmark legislation that will shape the future of AI in Europe and is expected to be the baseline for similar legislation in other countries. Here's how it impacts medical device manufacturers. |
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By Jim Welch and John Babitt, EY | Leaders from Ernst & Young deliver intel on the four biggest trends that impacted the medtech industry in 2024 that savvy medtech companies will seize for success in 2025. |
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| The Standardization Of Plastic Luer Fittings | White Paper | Nordson MEDICAL | This white paper aims to explore the significance and challenges of the standardization of plastic luer fittings and the importance in ensuring the quality and safety of medical devices. |
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| Cultural Audits: What Are They And Why Are They Essential? | Article | B. Braun OEM Division | The medical device industry is familiar with quality audits, but is less familiar with the benefits of having a cultural audit to assess the competence, dedication, and passion that each party brings to the table. |
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