Infection prevention and control are crucial for guaranteeing patient safety in operating theatres. When it comes to endoscopy, meticulous cleaning and high-level disinfection is needed to ensure clean and safe use of endoscopes, on subsequent patients.
Join Fujifilm Europe in Vienna, Austria, for new product launches, an MRI symposium, and a chance to meet our experts and learn how we can take on the healthcare challenge together.
Randomized, double-blind, placebo-controlled study to evaluate efficacy of novel pan-GI prokinetic in patients with gastroparesis Renexxion Ireland Limited, a private biopharmaceutical company committed to delivering innovative drugs to patients with high unmet need in gastrointestinal (“GI”) disorders, is pleased to announce that the first patient has been treated in Europe with naronapride, a potential best-in-class […]
Mawi is a complete cardiac monitoring solution created to streamline clinical workflow and profitability. These extended holter devices are single-use and disposable, with no need to assemble or charge. Mawi has 2, X-shaped vectors for sufficient detection of clinical pathologies, and to overcome signal-to-noise limitations, providing continuous uninterrupted data.
Juniper Research is pleased to announce that entries are now open for the Future Digital Awards for Digital Health Innovation 2023. Since 2008, the Future Digital Awards have been awarded to tech companies at the forefront of their respective fields. This includes companies delivering products or services which are innovative, have the potential to disrupt their ecosystems, and provide […]
The European Commission is proposing to give more time to certify medical devices to mitigate the risk of shortages. The proposal introduces a longer transition period to adapt to new rules, as foreseen under the Medical Devices Regulation. The new deadlines depend on the medical devices’ risk class and will ensure continued access to medical […]
The first US patient has been enrolled at MedStar Washington Hospital Center in the SELUTION4ISR study evaluating SELUTION SLR™ to support FDA approval. This milestone follows Investigational Device Exemption (IDE) approval in the US in October 2022. SELUTION SLR is the first sustained limus release coronary drug-eluting balloon (DEB) to receive FDA IDE approval for In-stent […]
Medical device provider Mindray has become one of the first manufacturers in the world to receive certification for its defibrillators, under the European Union’s newest Medical Device Regulation (MDR).
April 2024
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