The Quality Management System / Quality Assurance Department at Sana Med Pharmaceutical Company, in accordance with international models in this field, sets regulations, requirements, processes and documents that cover the various stages of the life of a pharmaceutical product. The application of this system is to improve the quality, facilitate innovation, continuous improvement of the company’s products and strengthen the relationship between pharmaceutical development and the company’s production activities. The quality assurance unit, as the most important supervisory and executive pillar located in the factory, is responsible for the periodic evaluation of the quality of the products with the approach of adapting the manufacturing process according to predefined codified methods.
One of the most important goals of the quality management system at Sana Med is as follows:
– Efforts to properly implement the principles of CGMP, GMP, GSP, GLP, ISO standards, PIC / S and…
– Establishment of productivity management system in different pillars of the company with the aim of optimal use of available resources, reduction of waste, environmental pollution, and production of quality products.
– Establishment of environmental management, safety and occupational health system through the implementation of relevant principles and standards.
– Preparation and compilation of processes, instructions, standard executive methods (SOPs), record keeping and… in order to ensure the full implementation of QMS. In a manner that all documents are carefully designed, recorded, distributed, maintained and reviewed in due time.