UK and Netherlands-based cyber security and compliance firm Naq has raised €6 million (£5.1m) to help health technology companies meet NHS standards.
The startup, which emerged from the government’s National Cyber Security Centre flagship cyber…
After a few mixed years in medical technology (MedTech) mergers and acquisition (M&A) activity, 2025 is shaping up to be a landmark year, particularly among cash-rich medical device strategics. In Q1 2025, there were 57 MedTech M&A transactions totaling $9.2 billion, compared to 62 deals worth $2.7 billion…
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8foldGovernance supports businesses to accelerate MedTech, Digital Health or Medical Service compliance, ensuring both product and business quality. The team join a host of subject matter experts as part of the RADIANT CERSI DigitalHealth.London…
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What You Should Know:
– Alphabet’s Verily announced in an internal memo that is has closed its medical device division and laid off staff. The exact number of employees affected was not revealed.
– According to…
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HIV self-testing (HIVST) allows people to test for HIV outside traditional health facilities, but this presents challenges around pre-and-post-test counselling, reporting results and linking to care. Digital interventions for HIVST, a type of software…
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Nancy Hairston, the President and CEO of MedCAD, a Dallas-based medical technology company built on an innovative approach to the design and production of patient-matched medical implants joins eHealth Radio and the Health News Channel….
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What You Should Know:
– Artera, the developer of multimodal artificial intelligence (MMAI)-based prognostic and predictive cancer tests, announced today that the U.S. Food and Drug Administration (FDA) has granted De Novo authorization for ArteraAI…
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HealthTech firm Sanome has gained regulatory approval for its AI warning system which predicts healthcare-associated infections (HAIs) by analysing patient data from electronic patient records (EPRs).
MEMORI has been approved by the Medicines and Healthcare…
We're excited to be back for another episode of the Life Sciences Today Podcast by Healthcare IT Today. My guest today is Julio Martinez-Clark, CEO at Bioaccess, a CRO that specializes in executing first-in-human…
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Ran Chen, CTO at Pure Global
In the past five years, medical device companies have faced continuous change, with new regulations, evolving standards, and increasing documentation requirements. The 2024 MTI Regulatory Report put it plainly:…
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