Quality Assurance (QA) are responsible for the Quality Assurance Programme, which assures Management that the regulatory studies performed at the Centre for Biopharmacy Research are in compliance with the principles of Good Laboratory Practice (GLP), Good Manufacturing Practice (GMP) or Good Clinical Practice (GCP) which are legally binding.
Quality Assurance documentation also serves to assure the Medicines and Healthcare products Regulatory Agency (MHRA), of the compliance of the regulatory studies performed at the Centre for Biopharmacy Research during their regular inspections.
Specifically, Quality Assurance verify study plans, perform study audits, process audits, facility audits, system audits and external audits. Final reports are audited for accuracy and compliance. Quality Assurance are available for consultancy and informal questions on any aspect of compliance.
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Last Updated 04/09/2008 14:07:00
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