Medical Device Registration in Qatar

Regulatory authority: Medical device registration in Qatar is conducted through 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, phytosanitary, and Islamic grounds by means of certificates. A local agent is required and must be registered.

Since February 28, 2011, only medical devices that have obtained a Qatar MEC marketing authorization may be sold unless they had already obtained authorization prior to that date. Moreover, after June 30, 2011 only Qatar MEC-authorized medical devices are allowed to be used within Qatar, while devices in use before that date may continue to be utilized.

Medical devices must be authorized by one of the founding members of the Global Harmonization Task Force (GHTF) to have access to the Qatar market.

As of 2012, Arazy Group now offers our new service, LICENSALE.COM. This unique, cloud-based application provides you, the medical or IVD device manufacturer, with a comprehensive service that results in the successful registration of your product in Qatar and ownership of the registration license through your company.

Once you register in Qatar through LICENSALE.COM, a global compliance profile is generated that easily facilitates the registration of your product in more than 80 countries around the world. LICENSALE.COM creates a foundation that makes registration simpler, faster, and more cost-effective than any alternative available today.

Get a Quote >

now with

Read More > at