Brighthills

At BrightHills, we specialize in custom software development for MedTech and other regulated industries. With 20 years of experience, we manage entire projects – from planning to compliant delivery – or provide just skilled professionals. Our expertise spans SaMD, medical devices, telemedicine, hospital & laboratory information systems, as well as data engineering, AWS cloud computing, and agentic AI development. We support the full software lifecycle (SDLC) and guide clients in establishing eQMS, providing consulting and documentation to meet regulatory requirements such as FDA 510(k), EU MDR, ISO 13485, and ISO 27001. Our 150+ experts have delivered 400+ projects across the EU and U.S, enabling safe, scalable, and innovative digital health solutions. If you are looking for a reliable partner in regulated software development, feel free to connect with us.