January 13, 2026 - PRESSADVANTAGE - In the highly regulated field of medical device labeling translation, ensuring that ...

Great Britain is entering a new era of MedTech regulation, with major pre-market changes expected that are designed to ...

Integrated Circuits Understanding radio protocols and requirements is the first step in successfully using wireless communication in medical applications. Carl Falcon Table I. Wireless system ...

Product design risks can be mitigated through digital commissioning strategies for device design that speed continuous design ...

In the unforgiving landscape of medical device development, where regulatory deadlines intersect with clinical imperatives and patient safety requirements, the successful navigation of a 510(k) ...

On February 2, 2024, the US Food and Drug Administration (FDA) published a much-awaited final rule: the Quality Management System Regulation (QMSR). 1 By issuing this rule, FDA amended the medical ...

The Federal Drug Administration’s current cybersecurity requirements are not appropriate for addressing and avoiding medical ...

The "Medical Device Regulations in the Middle East and North Africa Training Course (May 18th - May 19th, 2026)" has been added to ResearchAndMarkets.com's offering. The size of the medical device ...

The "Medical Device Regulations in the Middle East and North Africa Training Course (May 18th - May 19th, 2026)" has been added to ResearchAndMarkets.com's offering. The size of the medical device ...

Zibo Qichuang Medical Products Co., Ltd., a professional disposable medical consumables manufacturer based in China, continues to strengthen its presence in the global healthcare supply market by ...

Within the category of In Vitro Diagnostic (IVD) devices, IVD consumables are projected to experience the highest compound ...