Quality Assurance and Validation Department
It is an independent unit of the Company and it reports directly to the Director of quality and certification.
Department carries out the design, implementation, documentation and monitoring of the functioning of the quality system of production of the drugs, which ensures the implementation of enterprise policy in the field of quality and stable achievement of compliance of the production to GMP, ISO 9001 and ISO 14001. It provides introduction of Good Manufacturing Practice (GMP) and oversees its implementation. Carries out internal and external audits. Provides planning, organization and methodical management of the work on validation of individual sections, laboratories and the Company as a whole.
Technical qualification and validation abilities allow the sector to monitor and evaluate all production processes to be performed at the territory of the Company. Equipment in the possession of the department allows to monitor and evaluate the critical points of the production process.
Your message was successfully sent