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Medical Device Registration and Approval in QATAR
General country-specific regulatory information is provided on this page for medical device registration and approval in QATAR.
Last updated on November 1st, 2021.
Medical Device Regulations and Classification in QATAR
REGULATORY AUTHORITY: Central Drugs Standard Control Organization (CDSCO)
CLASSIFICATION SYSTEM:
Medical Devices: Listed Device/I/IIa/IIb/III
IVDs: A/B/C/D
TIMEFRAME: New full product registration will take a minimum of 6 months.
SPECIAL REQUIREMENT: Foreign manufacturing facility must be registered to and approved by NMRA. An on-site audit may be necessary, but NMRA would exempt on-site audit if the site had been inspected by a stringent regulatory authority or WHO.
For detailed device-specific compliance information for each market, including QATAR, to expedite the preparation of your medical device or IVD registration application.
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