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The document discusses Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP). It provides definitions of GLP and GMP, outlines their histories and reasons for creation. GLP was created by the FDA in 1978 and aims to ensure quality and correctness in laboratory studies through principles like proper operating procedures and record keeping. GMP was created to control quality variation in drug manufacturing and aims to consistently produce drugs that meet specifications through guidelines cove

Author

Shyam Sunder Pancholi

Language

EN