Utilization of a qualified radiation protection expert ensures thorough evaluation of current safety status and prospects of foreseeing adverse events, promotes general safety culture within companies and enables comprehensive consideration of regulatory requirements.
Quality assurance of medical devices enforces proper and intended device function, and enables anticipation and reaction to indications of faulty function, wear and device-induced misdiagnoses.
Clinical evaluation of medical devices entering market or modifying function or intended purpose ensures, by utilization of all available data, that proper function and benefits are to be gained, and that they outweigh any anticipated risks.