The Kanda BioTech Quality System consists of the Quality Control Department (QC) and the Quality Assurance Department (QA). The Quality System provides and maintains the cGMP quality system to support all aspects of biopharmaceutical product manufacturing and to fulfill all present regulatory requirements. we are experienced in the transfer of developed and/or validated methods to our customers

     QC Department provides testing for raw materials, in-process control, stability and release of finish product for Kanda BioTech’s clients. In addition, QC is responsible for the microbiological control of products and the production facilities

QA Department assures clients and management that for all projects conducted  under GLP or cGMP regulations, the facilities, equipment, personnel, methods, practices, records and controls utilized during each study/project are in conformance with the applicable regulations