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Atraverse Medical, a San Diego-based medical device company pioneering universally-compatible transseptal access technology, announced to ...
DHA R&D-MRDC researchers are applying the latest regulatory guidance related to AI to better carry out their mission to develop life-saving medicines.
Summit and Akeso report Phase 3 success as ivonescimab shows PFS gains in NSCLC trial, with new studies and collaborations underway.
Medical device makers must balance PFAS performance benefits with health risks, preparing for regulation by auditing ...
The bone graft incorporating rhBMP-2 has received FDA IDE approval for a pivotal clinical trial in spinal fusion ...
Grammy Award winning singer and songwriter Anthony Hamilton underwent a colonoscopy for the first time in his mid-20’s, right ...
Boston Scientific has proven itself to be a fierce competitor among three major cardiac device makers, with a track record of meaningful innovation and impressive operational chops. Even a prolonged ...
Symposium will also feature presentation on the BACKBEAT global pivotal study Orchestra BioMed is currently enrolling in strategic collaboration with Medtronic, plc (NYSE: MDT) ...
Short Summary The EU, UK, and USA each have distinct and evolving regulatory systems for medicines and medical devices, involving strict approval, surveillance, and market access requirements managed ...
1d
Vietnam Investment Review on MSNFDA Approves Minder® the First Implantable Continuous EEG Monitor in the USMELBOURNE, Australia and DALLAS, April 23, 2025 /PRNewswire/ -- Epiminder, a pioneering medical device and information solutions company, today announced that it has been granted FDA authorisation via ...
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