Morocco is going through a major overhaul of the health sector in the past 6 years, and as part of it, a list of reimbursable medical devices was published in 2008, which increases the number of reimbursable devices by 500%.

The Ministry of Health regulates the importation and registration of medical devices, through the Medical Device Advisory Committee. There is no special requirement for a specific classification system or previous foreign marketing approvals; however certain other documents, such as CFS and QMS certificate may be required. In the case of pre-used equipment it is also required to present an FDA clearance.  A local representative is required to submit the application form and accompanied documents. 

Our country specific (*) regulatory services in Morocco include:

Medical Device specific regulation strategy reports in Morocco, Medical Device Registration with Medical Device Advisory Committee, technical documents preparation, license holder and local Authorized Representative in Morocco, QSD registration and Arazy Group unique line of GlobaR - Global Regulatory Hub™ products.

GlobaR Dossier™
GlobaR - One World Process™
GlobaR Submission Center ™
Universal Authorized Representative™

Please fill in the following form, submit your inquiry or discuss it with one of our online specialists. Let's get your products registered in Morocco!

(*) Moroccan 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 services.