Medical Device registration in Qatar is done with the Ministry of Economy and Commerce (MEC),  followed by an application request to the Ministry of Municipal Affairs and Agriculture (MMAA) for an inspection of the premises (if applicable) , since business activities may not be undertaken in certain prohibited areas. Import controls are applied on sanitary, phytsanitary and Islamic grounds by means of certificates. A local agent is required and must be registered.

Medical devices, which are presently allowed on the Qatar market, may continue to be marketed, however, after February 28, 2011 only medical devices that have obtained an Qatar MEC marketing authorization may be sold. Moreover, after June 30, 2011 only Qatar MEC authorized medical devices may be put into service within Qatar, while devices in use at that date may continue to be utilized. 

Only medical devices that have been authorized by one of the Founding Members of the Global Harmonization Task Force (GHTF) will have access to the Qatar market. Our country specific (*) regulatory services in Qatar include:
 
Medical Device specific regulation strategy reports, Medical Device Registration with Qatar MEC, local Representative and certification holder for Medical Device manufacturers, Qatar FDA Technical documents preparation and Arazy Group’s unique line of GlobaR - Global Regulatory Hub™ products.
 
GlobaR Dossier™
GlobaR - One World Process™
GlobaR Submission Center ™
Universal Authorized Representative™
 
Please fill the following form and submit your inquiry or discuss it with one of our online specialists. Let's get your products registered in Qatar!

(*) Qatar Regulatory Affairs services are part of the diverse professional consulting services provided by Arazy Group and can be found thorough this web site and inquired on through our form or online chat service.