The essentials of the Moroccan regulatory framework for medical devices and their procurement.

Procuring medical devices in Morocco falls within a regulatory framework aimed at patient safety: registration, import conditions and vigilance obligations.

Registration and authorisations

Devices must meet applicable requirements and, in some cases, be registered. Working with a certified local manufacturer simplifies documentary compliance.

Import vs local manufacturing

  • Reduced lead times and logistics costs locally
  • Parts and after-sales availability
  • Easier compliant documentation
  • Support for national industry

Good buying practices

Require traceability, instructions and the declaration of conformity. A Moroccan ISO 13485-certified industrial partner secures the regulatory chain.