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Good Laboratory Practice (GLP) is a set of principles that guides how laboratory studies are planned, performed, monitored, recorded, reported and archived. This is different from laboratory safety standards (such as appropriate clothing). GLP helps to ensure the credibility and traceability of data submitted, thereby addressing the issue of non-reproducibility in many biopharmaceutical experiments. GLP is intended to minimise adverse drug effects and improve human health and environmental safety profiles. GLP also helps to improve accountability and precision of data through the transparent and detailed documentation of laboratory work while assigning responsibility at various steps in the experiment. In addition, the International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH) has mentioned GLP as a pre-requisite for the successful international registration of pharmaceuticals.
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