Wiebe Postma, PhD is a Sr Consultant and CRO Lead at Qserve group with close to a decade of experience in the medical device industry. A generalist with in-depth knowledge of the medical device regulations and clinical operations, his goal is to help manufacturers find practical solutions to clinical data collection and regulatory compliance. He has been involved in the setting up of pre- and post-market clinical investigations with medical devices in Europe, as well as clinical evaluation and post-market clinical follow-up planning for a broad range of devices and indications. In recent years, he had a leading role in the growth of Qserve’s CRO services.