In line with the Central Administration of Medical Devices (CAMD)'s efforts to facilitate and simplify the procedures for receiving applications,

We would like to inform you that all the following requests are now exclusively received through the MeDevice Electronic Platform:

Import Approvals for Diagnostic Reagents and Laboratory Devices.

Annual Import Approvals and their amendments.

Reagent Registration Files (Imported and Local).

Unified Procurement Authority (UPA) Files.

Essential Requirements:
Therefore, please review the essential requirements for each service, which are available via the following link:
Please be advised that failure to fulfill the essential requirements outlined in the link will result in the direct rejection of the application.