The documentation section is responsible for the inventory, registration, documentation, maintenance and archiving of all production and analytical production files after review and to ensure their integrity and completeness. It is also responsible for releasing the operations to the market after reviewing all processes and analyzes of the operations and ensuring their security and its occurrence within the permissible limits. All documents of the factory of standard methods and specifications, analytical methods, models and others relating to all parts of the factory and its departments and the registration and documentation of technical problems of varieties and complaints of customers and archiving. Global Pharma Company continuously improves quality through compliance and compliance programs that ensure strict compliance with the policies and principles of the company within the framework of an integrated quality framework. * Global Pharma Company obtained the ISO 9001 certificate in quality management system.