The quality of every tablet, capsule and bottle that we produce is integral to the life of the patients.
This is Polipharm’s general policy on product quality, with each employee keenly aware that every drug manufactured by us directly affects patients’ lives, our mission and responsibility to continue to assure the stable supply of high-quality pharmaceutical products. To achieve this, Polipharm consistently strives for quality through its introduction of a robust management system that all processes from API and formulation research to production and distribution. Each person in Polipharm is accountable for ensuring product quality, and patients and consumers safety.
Polipharm’s business is performed in compliance with International standard i.e. GMP (PIC/S), ISO 9001 : 2008, ISO/IEC 17025 : 2005
Polipharm has state – of – the – art manufacturing facilities and used advanced testing instrumentation to guarantee the qualities of our products. After registration approval and start for routine manufacturing, quality is preformed throughout the process, for both active and inert ingredients, work in process and finished products.
Quality doesn’t end when the product released. Polipharm continues to monitor our products throughout the shelf life by stability study with zone 4B climate to ensure that products remain safe and effective throughout their shelf life.