On 25 June 2019, the University Medical Center Utrecht will organize a seminar on the new In-vitro Diagnostic (IVD) Medical Device Regulation (2017/746) essentials and implications of the new regulation for healthcare professionals working with IVDs. Factory CRO for Medical Devices and IVDs Director Clinical Operations Niels van Tienen will be present at this meeting to discuss performance evaluation and performance studies for IVDs, including an in-depth overview of the new ISO 20916:2019. Click here to get in contact with us!