Quality Assurance

Pasteur & Fleming Pharmaceuticals (Pvt).Ltd has the latest analytical instruments in our quality control department to monitor quality assurance through standard systems that to make sure quality of our products. A highly qualified and trained team of scientists, pharmacists, chemists, and Microbiologists work in our Research and Development and Operations department to develop new products in an environment that consistently improves the quality. At Pasteur & Fleming Pharmaceuticals (Pvt).Ltd we have always believed in continuous R&D towards the development of new pharmaceutical formulations. Our new product development program generally includes pre-formulation studies, excipient studies, analytical methods development, validation, formulation development and optimization, formal stability studies and manufacturing process development. We have a quality program dedicated to the continuous improvement of product quality of running products.

Production Departments

A production department is a group of functions within a business that is responsible for the manufacture of goods. Key roles are Selection of product and design. Production planning and control.
Machine maintenance and replacement. Production operations are carried out under the supervision of qualified and experienced technical staff, Production plants are known to manufacture a varied range of pharmaceutical products in India like generics, medications, supplements, medical devices, etc. These are produced as per certain guidelines and global policies as they drive the access to improve healthcare and medical facilities. Pasteur & Fleming Pharmaceuticals production department having two main plant Health & OTC Division (Nutraceuticals) and Pharmaceuticals Division. Nutraceutical division having Tablets & Liquid section while Pharmaceuticals division having a General Tablets, Dry Powder, Capsulation, Hormonal, Ophthalmic ointment & cream section and we are adding further section such as psychotropic, General Sachet, Injectable etc.

Quality Control Department

To ensure that all products and services offered to our customer consistently conform to all applicable regulatory requirements and with the principles and guidelines of current Good Manufacturing Practice (cGMP) to ensure a “fitness for use” expected by our customers’ contractual expectations. Furthermore, it is our policy to ensure that our facilities and our product development, manufacturing and logistics processes that affect the quality of the final medicinal product, are identified and controlled to provide a high degree of assurance that all commercial products consistently meet their pre-defined specifications and quality attributes.The dispatch of finished goods for sale /distribution can be planned only after authorization for Release after approval by Quality Control department/Assurance department.