Ministry of Health (MOH) in Jordan oversees the laws and regulations of the entire healthcare sector through the Jordanian Food and Drug Administration (JFDA) and several other bodies like the Royal Medical Services (RMS), Jordan University Hospital (JUH) and King Abdullah University.
A product needs to be approved by the authorities of US, Europe or Japan before it receives marketing authorization in Jordan. Classification system is similar to the EU’s device classification (Classes I, IIa, IIb, III). In most cases, there is no need for a local representative to register your product in Jordan.
Our country specific (*) regulatory services in Jordan include:
Medical Device specific regulation strategy reports, Medical Device Registration with Jordanian MOH, Certification holder for Medical Device manufacturers, Jordanian MOH 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 Jordan!
(*) Jordanian 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.
