The  GLP Formula France  (for  Good Laboratory Practice )  is a set of quality principles governing the organization of non-clinical health safety studies. These principles guarantee the reliability, integrity and traceability of the data generated. In France, the implementation of the GLP is strictly regulated, particularly for trials conducted in the pharmaceutical, agrochemical, cosmetic and industrial chemical product sectors.

GLP was introduced in the 1970s by the OECD (Organisation for Economic Co-operation and Development) to address concerns about the validity of test data. The main objective is to ensure that studies are conducted to high standards,  thus enabling regulatory authorities to assess risks to human health and the environment .

In France,  the National Agency for Food, Environmental and Occupational Health Safety (ANSES)  and  the National Agency for the Safety of Medicines and Health Products (ANSM)  are responsible for the inspection and monitoring of laboratories subject to the GLP.

The establishments concerned must meet strict criteria, including:

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