SUBMIT INQUIRY
Qatar
General country-specific regulatory information is provided on this page. Become a LICENSALE.COM user to receive detailed device-specific compliance information for each market, free of charge, to expedite the preparation of your medical device or IVD registration application.

REGULATORY AUTHORITY
: Medical devices in Qatar are managed by the Ministry of Economy and Commerce (MEC). Currently medical devices do not require registration, and only an import permit is required.

CLASSIFICATION SYSTEM: Medical devices are classified according to EU model into risk-based Classes I, IIa, IIb, III, and IV.

AUTHORIZED REPRESENTATIVE: A local authorized representative is required to obtain an import permit.

ADDITIONAL INFORMATION: Medical devices must be authorized by one of the founding members of the Global Harmonization Task Force (GHTF) to obtain market access.

Last updated on March 17 2015.



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