The two bodies regulating medical device registration in Lebanon are The Drug Import and Export Department and The Sanitary Engineering Service, which both act under the Ministry of Public Health. The Lebanese authorities accept all classification systems, and the type of product dictates the procedure it must undergo before receiving marketing authorization.

The registration procedure must be carried out by a local representative. Our country specific (*) regulatory services in Lebanon include:

Medical Device specific regulation strategy reports in Lebanon, Medical Device Registration with the Drug Import and Export department, The Sanitary Engineering Service and Ministry of Public Health, Technical documents Preparation, license holder and local Authorize Representative in Lebanon, 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 and submit your inquiry or discuss it with one of our online specialists. Let's get your products registered in Lebanon!

(*) Lebanese 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.