Whether developing new medical devices or improving existing products, our cross-disciplinary teams of specialists, researchers, EU MDR, designers, and engineers tap into expertise derived from multiple industries and technologies. Bringing a complete portfolio of design, prototyping, simulation, testing, and development under one roof, our fully merged development cycle enables us to offer an optimized design control package in line with FDA policies for medical device design and development for components and assemblies.
Our design and development engineers boost your idea from concept to completion, including, in the process, the most sophisticated methods and technologies in the medical device industry. At Seisa, we diligently conduct reviews, hazard identification, and risk analysis throughout our documented process.
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