The General Department of pharmaceutical Licenses (pharmaceutical factories department) responsible for editing licenses for pharmaceutical sites” pharmaceutical drug- veterinary-biological-cosmetics-appliances" after visiting the factory by many committees to ensure that the factory comply to most recent requirements of current GMP according to WHO requirements for pharmaceutical institutes to insure the safety and unity of all pharmaceutical products delivered to patients .
Workflow for licensing of Manufacturing Sites
Workflow for Licensing a New Production Line
Workflow for licensing Warehouse (added to a manufacturing site)
Workflow for changing Manufacturer's Name Company Representative Ownership Transfer
Guidelines for Obtaining a Typical Copy of Factory License
Pharmaceutical factories cancellation decrees