Morocco
REGULATORY AUTHORITY: Medical devices are regulated through the Bureau of Medical Devices, a division of the Department of Medicine and Pharmacy.

CLASSIFICATION SYSTEM: There is no special requirement for a specific classification system or previous foreign marketing approvals. However, certain documents, such as CFS and QMS certificates, may be required. In the case of pre-used equipment, it is also required to present FDA clearance.

TIMEFRAME: Licenses issued in Morocco are valid for five years.

AUTHORIZED REPRESENTATIVE: A local representative is required.

Last updated on March 17 2015.



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For​ more information on registration in Morocco, check out the following articles on our blog:
Country at a Glance: Morocco
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