Syria has very little domestic production and relies heavily on imports from China, India and West Europe. Regulation is conducted by the Directorate of Medical Equipment and Consumables, under the Ministry of Health. The registration procedure requires a CE mark or FDA clearance, CFS from country of origin, and other requirements. However, the procedure is not required to be carried by a local representative.

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

Medical Device specific regulation strategy reports in Syria, Medical Device Registration with Directorate of Medical Equipment and Consumables, the Ministry of Health, technical documents preparation, 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 Syria!

(*) Syrian 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.