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    TheUKGood Laboratory Practice Monitoring Authority(2000) Guide toUK GLP Regulations 1999, MHRA, London, UK.–A useful guidance document for the UK. 6. The MHRA grants permission for clinical trials to be conducted in the UK in accordance (Regulation) The Good Laboratory Practice Regulations 1999 (S.I.
    fileslib. Regulatory guidelines by Medicines and Healthcare products Regulatory Agency- UK MHRA including GMP – Orange Guide, Validation, GLP etc.in pdf format.
    In the UK these requirements are contained within The Good Laboratory Practice Regulations 1999 as amended by The Good Laboratory Practice Missing: guide | Must include: guide
    Who regulates GLP in the UK? The test facility must belong to the UK GLP compliance monitoring programme, run by the UK GLP Monitoring Authority (UK GLPMA ) .
    What are the GLP guidelines? The principles of Good Laboratory Practice (GLP) define a set of rules and criteria for a quality system concerned with the organisational process and the conditions under which non-clinical health and environmental safety studies are planned, performed, monitored, recorded, reported and archived.

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