Navigate the clinical requirements for your medical device
TÜV SÜD’s Clinical Affairs specialists have the experience and the expertise to understand the needs of you and your customers regarding safe medical devices and patient safety. Our team of in-house medical doctors have more than 30 years of experience in the voluntary review of clinical assessments for clients.
Aware that market pressures demand quick timelines, our scientists, professors and medical doctors work efficiently to assess your evaluation of clinical data based on clinical studies that meet market needs and regulatory requirements. Through the benefit/risk ratio evaluation of a given device, we understand the potential side effects, treatment technology and the proof of data.