Chris Whitehouse, a political consultant and expert on medical technology policy and regulation at Whitehouse Communications looks at the potential effects of value-based procurement.
Claire Ryan, global head of QA/RA, Joanne Cross, director of marketing and Jennifer Golding, product manager at Yourgene Health discuss the in vitro diagnostic regulatory landscape in Europe and how the ongoing changes will help improve safety.
Following TekniPlex Healthcare’s acquisition of Seisa Medical, Med-Tech Innovation News spoke to Chris Qualters, CEO of TekniPlex Healthcare, to find out more about the deal.
Thirona, a company specialising in advanced analysis of thoracic CT images with artificial intelligence, has received U.S. Food and Drug Administration (FDA) 510(k) clearance for the latest update of its AI-based clinical software LungQ (v3.0.0).
Duncan Hand, director of the Medical Device Manufacturing Centre explains why an integrated ecosystem, combined with natural innovative spirit, are essential to the future of Scotland’s medical device manufacturing sector.
Stäubli’s Training Manager, Mik Bloor, looks at how a greater understanding of the way in which robot programs have been structured can lead to opportunities to optimise robot trajectories or simplify the program.
Over the past 16 years Wideblue has worked with scores of medical device manufacturers on helping them bring their innovations to market. During this time two things have stood out — the importance of prototyping and testing.
Juha Saily, regional development manager, Helmee Imaging, highlights how new vision technology enables automated in-process inspection of medical devices with high gloss, specular and clear surfaces.
