We have invested considerably in ensuring reproducible quality in our laboratory. Analyses of all clinical studies are conducted on the backbone of the quality management system we have developed. We provide training in quality management, and we continue to improve validation procedures, and to innovate in laboratory management and sample storage and sample tracking. We are trying to influence international regulatory guidelines by suggesting optimal design of validation experiments as well as suggesting strategies for successful analysis of clinical studies. We are hoping to establish an international network of inter-laboratory quality control and assurance schemes so that results from one laboratory can be compared directly with results from another.
Our quality management system covers all laboratory activities and includes:

➢ Procedures for validation of bioanalytical methods
➢ Procedures for receiving, logging, storing, analysing and discarding clinical samples
➢ Procedures for Data storage, Data backup, Data transfer and Data reporting.
➢ Procedures for Ordering, Receiving, Storing, Using and Discarding consumables and chemicals
➢ Procedures for Ordering, Receiving, Storing, Using, Maintaining, Calibrating and Discarding Instrument and Equipment
➢ Procedures for monitoring and controlling temperatures and laboratory environment

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