ETHOS Health was established in 2014 with a clear vision: to facilitate the introduction of innovative and disruptive solutions into healthcare systems, obtaining FDA, CE Mark, or EMA approvals. The objective is to improve and sustain healthcare for those who use and implement it. As a leading boutique consultancy firm, ETHOS Health offers a range of services to startups and corporations in biotech, medtech, and healthtech. Our expertise covers regulatory affairs, commercial strategy, corporate strategy, and engineering, among others. Our team has extensive experience working in management positions in the NHS. We have written clinical safety standards, policy and guidelines for the UK NHS public healthcare system, and international standards for health software including medical devices. Currently, we provide consultancy work for the NHS, which is one of our most valued customers. We can offer support throughout the product journey, from MVP design to commercial execution, providing us with a competitive edge. We have worked closely with notified bodies like SGS, BSI and Tüv Sud to achieve CE Mark and collaborated with executives from major pharmaceutical and medical device companies. This enables us to align your regulatory and commercial strategy to enhance product adoption once CE Mark is granted.