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 and In Vitro Diagnostics. Our strong international team, located in Europe, China and the United States, combines their broad range of knowledge and expertise in medical devices and IVDs, to assist manufacturers in gaining market access around the world. Qserve’s in-house consultants advise in numerous areas, including Regulatory Affairs, EU-MDR, EU-IVDR, FDA Compliance, Global Regulatory Strategy, Clinical Affairs, CRO, Strategic Planning, Due Diligence & GAP analysis, CE-Marking, Pre-IDE, PMA, 510(k) Submissions, us Agent, EU representative, UK RP, China Agent, NMPA Registration, Global Medical Device Registration, Trainings & Quality Management Systems implementation. Your Global MedTech Partner for Regulatory Affairs, Quality Assurance and Clinical Trials. Your global CRO for Medical Device Clinical Trials