… and why you should join us on March 19th, 2020 in Brussels, Belgium.
The MedTech Meetup is unique in Belgium because it is the only event with an exclusive focus on medical devices. Its goal is to gather the Belgian medtech ecosystem in order to give its stakeholders the opportunity to meet and to learn from each other.
Esther Daemen, Training and Quality Director at TRIUM, will give a clear understanding of how the MDR and the upcoming update of the ISO14155 will impact clinical trials.
The MDR becomes effective in May 2020 and an updated ISO 14155 standard is also expected soon. If you wonder what this means and how big the impact will be on your device related clinical trials, then join this session. A mix of theoretical background and real-life examples will be shared and discussed, ensuring you a good head start towards compliance.
Don’t miss her workshop on March 19 and register here !