Learn all aspects of the MDR and its application to regulatory approval of your medical devices
We offer a range of training events to familiarise stakeholders from across the industry to all aspects of the new MDR. Our events are targeted for:
- Product Specialists
- Regulatory Managers
- Anyone who wants to learn more about the new regulations
Due to the current coronavirus pandemic, our live seminars have been transitioned to our online workshops. When restrictions are lifted enough, we will run live seminars again. Sign up to our newsletter to get email notifications when we open new events.