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)
Medical Devices: Listed Device/I/IIa/IIb/III
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.
Please fill out your contact information so we can better assist you.
* Note: If you use your general ISP e-mail address, such as gmail, yahoo etc. your LinkedIn profile address is required to process your request.