Qserve Group

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

Company’s Keywords:

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, eumdr expert, training