MEDVIA, UZ Antwerpen and Health Hub Aalst are hosting a workshop for healthtech innovators on navigating ethical documentation.
With the rise of legislation for medical devices, such as the In Vitro Diagnostic Regulation (IVDR) and the Medical Devices Regulation (MDR), it is becoming increasingly essential for developers of medical technologies to know when and why medical ethics dossiers should be submitted, what should be included and who should be involved. Beyond just compliance with laws, it’s important to ensure the safety and ethical integrity of medical technologies.
Navigating Ethical Approval
7 June 2024, 9.30-13.30
HealthHub Aalst
Capucienenlaan 93A, Aalst
Iris Verhaegen of UZ Antwerpen’s Clinical Trials Center (CTC) will lead the workshop. CTC acts as the first point of contact for coordination and support of clinical studies and scientific projects, making it a valuable source of guidance and expertise for setting up such dossiers.
