What will the industry face or achieve in 2025? These trends will be critical in medical device cybersecurity.
MDR Certification Strengthens Resyca’s Leadership in Soft Mist Drug-Device Combination Products ENSCHEDE, NL / ACCESS ...
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Six months “a very limited window” for medical device shortage flaggingBeta CEO Marcel Botha talks about the FDA’s plans for medical shortage notifications and how Trump’s policies may impact US ...
A supercapacitor made from sargassum seaweed nanofibers powers medical devices inside the body, kills bacteria, and naturally ...
The FDA is urging Congress to implement mandatory medical device shortage reporting to address growing vulnerabilities in the ...
The Medicines and Healthcare products Regulatory Agency (MHRA) has issued a suite of guidance specifically designed to help medical ...
The MHRA has issued fresh guidance to help medical device manufacturers prepare for upcoming regulatory changes.
As medical devices become more complex, and as regulatory requirements become more rigorous, it’s imperative that medical devices using electronic components are developed as efficiently as possible.
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OCT Medical Devices 2025: biggest regulatory requirement issues ‘start at the site level’When conducting a clinical investigation, meeting regulatory requirements is predicated on factors such as the quality of ...
IntroductionIn the rapidly evolving healthcare landscape, medical devices play a pivotal role in enhancing patient care and improving health outcomes. The road to getting these devices from concept to ...
The new director of the FDA’s device center contrasted a European rule with the lack of mandatory reporting requirements for ...
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