TechMed Workshop Series 4/6: Medical devices: controlled from design to production

In order to market medical products, many requirements must be met. Within the European Union, these requirements are imposed by Medical Device Reporting (MDR), formerly known as Medical Device Directive (MDD).

You are invited to participate in workshop nr 4 from the series: ‘Remove the barriers to market readiness’. This workshop focuses on the business aspects and legal requirements that are imposed on the development of new medical devices, for example the MDR, production, service, setting up a supply chain and transport of medical devices.

The workshop will be held by the TechMed Proeftuin partner Unitron Group.

For more information and registration, please visit the TechMed Events website.