Despite the significant progress Yemen has made to expand and improve its health care system over the past decade, the system remains severely underdeveloped. However, a serious infrastructure of work has been carried out over the past few years in order to improve the healthcare system and the regulations involved.

The Ministry of Public Health and Population (MPHP) regulates medical devices through the Supreme Board for Drugs & Medical Appliances (SBDMA). The application should include a CFS for the device in question, GMP certificate and other documents. The application should be carried out by a local representative.

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

Medical Device specific regulation strategy reports in Yemen, Medical Device Registration with the SBDMA and MPHP, 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 Yemen!

(*) Yemeni 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.