One area that medical device manufacturers often overlook in post-market surveillance (PMS) planning for EU MDR and EU IVDR ...
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Hosted on MSNThousands left with untested drugs and medical devices in bodies after Trump order: reportReal-life consequences over President Donald Trump’s plot to dismantle the U.S. Agency for International Development are emerging as the agency’s stop-work order has left thousands of people with ...
CMOs can solve challenges with state-of-the-art equipment and expertise, explains Henri Asselin at Beacon MedTech Solutions.
Early alignment and test planning derisks commercialization of high-performance optical devices, says Minnetronix engineer ...
At MD&M West, PIA will give attendees live demonstrations of its assembly technology, including V-RAC. In Booth 5328 in the ...
Similarly, when medical device manufacturers require automated assembly systems for complex applications, they, too, turn to ...
Medical Devices conference, held in Munich, Germany on 28-29 January, was filled with sessions that dug into the minutiae of ...
Abhishek Pandurang Benke led the development of an innovative cardiovascular diagnostic device, improving accuracy, speed, ...
Barry Datlof, MTT’s chief of business development and commercialization, received the 2024 DOD Linsteadt Technology Transfer ...
Engaged BSI Group to start the process of obtaining regulatory clearance of the MODD1, next-generation insulin pump for the European market- Targeting Q1 2026 for expected clearance of the MODD1 in th ...
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GlobalData on MSNOCT 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 ...
Expands the standard off-the-shelf power supply line to 660 W, certified for cardiac applications, allowing medical device ...
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