Good clinical laboratory practice (GCLP) is a GxP guideline for laboratory samples from clinical studies.
Good clinical practice (GCP) does not define requirements for laboratories and good laboratory practice (GLP) focusses on pre-clinical analyses and not on human samples from clinical trials. The Research Quality Association (RQA) suggested in 2003 a guideline to close the gap. Later the World Health Organization and the British Medicines and Healthcare products Regulatory Agency issued their own versions of a GCLP guideline.
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SAFETY ELEMENTS IN MEDICAL LABORATORY PRACTICE
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Good Clinical Practice (Lecture-48)
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Good Laboratory Practice - GLP Overview Training
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Literature
- WHO Good Clinical Laboratory Practice (GCLP) ISBN 978-92-4-159785-2
- Stevens W. (2003) Good Clinical Laboratory Practice (GCLP): The need for a hybrid of Good Laboratory Practice and Good Clinical Practice guidelines/standards for medical testing laboratories conducting clinical trials in developing countries. Quality Assurance, 10: 83–89.
- Grant, Vanessa and Stiles, Tim, Research Quality Association (2003 and revised in 2012), Good Clinical Laboratory Practice ISBN 978-1-904610-21-2
External links
- WHO Good Clinical Laboratory Practice (GCLP) (11 Oct 2010)
- MHRA guidance on the maintenance of regulatory compliance in laboratories that perform the analysis or evaluation of clinical trial samples (11 Oct 2010)
- Research Quality Association (RQA)
- Good Clinical Laboratory Practice (GCLP)
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This page was last edited on 15 September 2023, at 09:29