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Thermo Fisher Scientific has increased its takeover offer for Qiagen, after its original offer was reportedly criticised by some shareholders as being undervalued. Under the revised offer, Thermo
Abiomed has secured approval from the US Food and Drug Administration (FDA) for one-way digital data streaming during patient support from Automated Impella Controller (AIC). AIC is the
Ascend Performance Materials is seeking clearance from the US Food and Drug Administration (FDA) for its Acteev technology in a pair of surgical masks to protect against SARS-CoV-2.
Medical imaging company Sectra has expanded its partnership with Region Västmanland in Sweden to deliver a digital pathology solution. The Swedish healthcare region already uses Sectra’s software for
Arterys, a leading global medical imaging platform to deliver clinical AI products over the internet, just received its seventh USA FDA clearance and announced its latest round of funding —
-LetsGetChecked, the leading direct-to-consumer at-home health testing and insights company, announces today the authorization of the new Coronavirus (COVID-19) Sure-track Test for at-home consumer use by the U.S.
Since the installation of one of the first two commercially installed SLA 1 machines at Baxter Healthcare in 1988, medical applications have been a leader in applying
Tokyo-based Astellas Pharma has acquired a privately held development-stage biotechnology company Xyphos Biosciences in a deal worth $650m. The acquisition enables Astellas to gain Xyphos’ proprietary Advanced Cellular
Chicago-based Augmedics has secured the US Food and Drug Administration (FDA) 510(k) clearance for its xvision Spine system (XVS), an AR guidance system to be used in surgery.
GE Healthcare has unveiled the Edison developer programme in a move to help integrate artificial intelligence-driven applications into existing healthcare workflows. The developer programme is based on the