In a recent MD+DI webinar called, “Understanding the EU MDR”, which was sponsored by Accumold, Nelson Laboratories, and Oliver Healthcare Packaging, Dr. Bassil Akra, CEO of Akra Team GmbH, gave ...
LONDON – Long-awaited guidance on how software will be treated under the stricter EU devices regulations brings clarity but also adds to the mountain of preparations needed to comply with the new ...
Prioritizing compliance with European Union Medical Device Regulations (EU MDR), especially for legacy products, can be daunting, despite the extension of EU MDR deadlines from 2026 to 2028. To ...
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