Qserve is your global partner for Medtech Regulatory, Clinical & Quality Compliance and your CRO for Medical Device Clinical Trials. With our broad range of knowledge and experience, we can support you with getting market access all over the world and for all kind of Medical Devices. Our strong international team, located in Europe, China and the United States, combines their broad range of knowledge and expertise in medical devices, to assist manufacturers in gaining market access around the world. Qserve’s in-house consultants advise in numerous areas, including Regulatory Affairs, Clinical Affairs, CRO, Strategic Planning, Due Diligence & GAP analysis, CE-Marking, Pre-IDE, PMA, 510(k) Submissions, US Agent Representation, CFDA Registration, Trainings & Quality Management Systems implementation. Your global partner for Medical Device Regulatory Compliance Your global CRO for Medical Device Clinical Trials