At Purelife Bioscience Co., Ltd, Quality assurance is inherent in every procedure of our manufacturing, since we work by the standard of GMP regulation, quality is considered foremost throughout our business activities. Our quality system is composed of Quality control department and Quality Assurance department. They ensure compliance to GMP standards with quality management systems encompassing activities such as documentation, quality control, validation (Plant, equipment and computer system), audit and regulatory document submissions.
ISO9001:2000 standard was strictly complied while the concept of current Good Manufacturing Process (cGMP) has been carried out for all the process from raw material procurement, production control, quality analysis to products release and after service. Standard Operation Procedures (SOPs) are established throughout each production process, from raw materials purchasing and production through to product distribution. Completed SOP files was established by QA department and performed strictly in the whole factory.
Additionally, Purelife Bioscience also collaborates closely with some authoritative third party laboratories to guarantee the top quality of all materials, such as Eurofins, Wessling, Intertek etc .
