From the simplicity of a syringe to the complexity of a pacemaker, medical devices are subject to high regulations and standards to meet market-specific quality, safety, and performance standards.
Our experts in the field deliver a wide range of standard and non-standard testing and certification such as CE or FDA through partnership with notified bodies that train and guide each stage of product design from the lab to the shelf.


At the center of clinical decision making and treatment pathways across the medical sector, together with our partners we provide help ensure compliance, quality, and safety in your product line through patient-centered innovation built on a model of health and care.