Adaptive unveils data of MRD assessment test in blood cancer treatment
Adaptive Biotechnologies has unveiled new data highlighting the significant role of measurable residual disease (MRD) assessment in the treatment of …
Adaptive Biotechnologies has unveiled new data highlighting the significant role of measurable residual disease (MRD) assessment in the treatment of …
Immunovia’s next-generation in vitro diagnostic (IVD) for early-stage pancreatic ductal adenocarcinoma (PDAC) has shown promising results in a clinical evaluation …
Copan Diagnostics has received the US Food and Drug Administration (FDA) clearance for its urine collection and transport system, UriSponge. UriSponge …
Sonic Healthcare has signed binding agreements to acquire Germany-based Laboratory Group Dr Kramer & Colleagues (LADR), for an enterprise value …
Zynex has completed the clinical verification trial of its pulse oximeter, NiCO, marking a significant milestone towards the Food and …
Nua Surgical has concluded a €6.5m Series A funding round to advance its caesarean surgery (C-section) assistance device. The Irish medical …
Cleerly has concluded a $106m Series C funding round to advance its AI-driven coronary artery disease (CAD) platform. The US-based digital …
Spine device company Zavation Medical Products has appointed Lane Major as its new chief executive officer (CEO). With more than two …
The concept of extremely long life, popularised in films like Highlander, may seem like pure fiction, however; researchers are actively …
Last month, Veeva announced multiple generative artificial intelligence (genAI) capabilities in its Vault CRM such as Vault CRM Bot and …
RenovoRx has begun commercialising its RenovoCath device after receiving the first purchase orders for the delivery platform, which was cleared …
The UK's Medicines and Healthcare products Regulatory Agency (MHRA) has selected five technologies for its AI Airlock pilot scheme. The scheme …
US-based Field Medical has secured breakthrough device designation from the US Food and Drug Administration (FDA) for the FieldForce ablation …
Surgical innovation is entering an era constrained less by technological limitations but facing challenges in regulation, economics, and expertise. In …
Zimmer Biomet has secured the US Food and Drug Administration (FDA) 510(k) clearance for its total knee implant component, Persona …