(IN BRIEF) The European Association of Percutaneous Cardiovascular Interventions will hold its first official summit under the European Society of Cardiology in Munich on 19–20 February 2026, bringing together leading and emerging specialists in interventional cardiology to focus on education, … Read the full press release
Posted in Business, Education, Financial, France, Healthcare, Industrial, Investment, Management, News, Pharma & Biotech, Science, Technology
Tagged Alaide Chieffo, cardiology education, Cardiovascular Imaging, catheter-based procedures, clinical guidelines, EACTS, EAPCI, ESC, ESC and EAPCI convene multidisciplinary summit to shape the future of catheter-based cardiovascular care, European Society of Cardiology, heart failure, Heart Team, interventional cardiology, Medical Device Regulation, Munich, patient-centred care, PCI, percutaneous cardiovascular interventions, simulator training, TAVI, Thomas F. Lüscher, young professionals
(IN BRIEF) DNV has certified Clearlab’s contact lenses and multi-purpose lens care solutions under the Medical Device Single Audit Program, ISO 13485, and the EU Medical Device Regulation through a parallel audit process. This integrated approach enabled Clearlab to achieve … Read the full press release
Posted in Business, Healthcare, Industrial, Management, News, Norway, Pharma & Biotech, Technology
Tagged Asia Pacific, Clearlab, contact lenses, DNV, DNV Certifies Clearlab Contact Lens Products Under Global Medical Device Standards, DNV Completes Parallel Audit for Clearlab Contact Lenses and Lens Care Solutions, EU MDR 2017/745, Europe, Global market access, ISO 13485, lens care solutions, MDSAP, medical device certification, Medical Device Regulation, medical devices, parallel audit, patient safety, quality management systems, regulatory compliance
(IN BRIEF) SGS Belgium NV has been officially designated by the European Commission and Belgian Competent Authority as a Notified Body (NB) under the In Vitro Diagnostic Medical Device Regulation (IVDR), EU 2017/746. This milestone enhances SGS’s ability to support … Read the full press release
Posted in Belgium, Business, Financial, Healthcare, Industrial, Investment, Management, News, Science, Switzerland, Technology
Tagged Belgium, certification, compliance, EU, EU IVDR, FAGG/AFMPS, Geofrey De Visscher, In Vitro Diagnostic, ISO 13485, IVDR, MDSAP, medical device, Medical Device Regulation, Notified Body, partnership, patient care, Regulation, SGS, UKCA
EuropaWire (EW) is the first truly pan-European and leading press release distribution and newswire service for Europe and the European Union working towards consolidating Europe’s voice on the global newswire and media scene. The newswire service comes with advanced submission forms, flexible pricing and PR budgeting, granular targeting, nearly uncapped reach across countries, markets, verticals, industries, audiences, languages, etc., translation and localisation for greater local PR impact, in-depth distribution reporting, metrics and insights including measured PR reach, reads, engagements, impact, etc., no cap on words, images and multimedia to go along with your release, among others. Your press releases will be seen among the releases of Europe’s biggest and most prominent companies, brands and institutions. Here you can learn more about EuropaWire’s mission, achievements, services, etc.
HOW TO GET STARTED?