Quality Control is the part of Good Manufacturing Practice refers to the sum of all procedures and activities undertaken to ensure the quality, safety and efficacy of the pharmaceutical products meet the regulatory and customer requirements before released for sale, through sampling and testing of incoming raw materials, packaging materials and finish pharmaceutical products using standardized laboratory instruments and validated testing methods.
Quality control mission is to monitoring the quality of the incoming raw materials, packaging materials and finish pharmaceutical products with accurate test results, timely, high quality and cost / benefit ratio, meeting the requirements of the latest pharmacopoeial references.
Quality control policy is achieved through:
- Suitable continuous improvement environment.
- Professionals / Highly-qualified personnel
- Using standardized modern analytical instruments and validated testing methods as the latest pharmacopoeial to provide the most precise and accurate results.