The General People's Committee for health and environment is responsible the regulation and monitoring of all health services in Libya. The registration procedure is conducted as part of an annual purchasing program of the government system for imported pharmaceuticals and medical devices. The importer should submit an application, accompanied by several certificates and other documents, such as GMP and ISO certificates. The process should be carried out by a local representative.

The Libyan authorities accept all classification systems.  Our country specific (*) regulatory services in Libya include:

Medical Device specific regulation strategy reports in Libya, Medical Device Registration with The General People's Committee for Health and Environment, technical documents preparation, license holder and local Authorized Representative in Libya, 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 Libya!

(*) Libyan 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.