Good Laboratory Practices Programmes
Good Laboratory Practice (GLP) programme deals with successful application of good laboratory practices to ensure that laboratory testing is designed, performed, supervised and reported in an organized and controlled manner. GLP plays a vital role to guarantee the consistency, reliability and reproducibility of results and the safety and efficacy of the product.
These programmes focus on the requirements of the Good Laboratory Practice (GLP) regulations imposed by the Food and Drug Administration (FDA), international rules for GLP studies (primarily OECD regulations). The programmes also includes facility and equipment requirements, documentation requirements, roles and responsibilities, outsourcing relationships along with practical examples that are used to highlight key aspects of the regulations.