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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. Qserves in-house consultants advise in numerous areas, including Regulatory Affairs, EU-MDR, EU-IVDR, FDA Compliance,...
Medical device regulatory compliance,medical device global registration,medical device clinical evaluation,medical device quality assurance,medical device auditing,medical device training,medical device regulatory affairs,medical device cro,eu-mdr expert,training,eu-ivdr expert,medical device registration partner,us fda compliance partner,local agent services,global regulatory strategy,in vitro diagnostics ,and companion diagnostics
Qserve group operates in the Business consulting and services industry.
Qserve group's revenue is 11m - 100m
Qserve group has 51 - 200 employees.
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