GLP Certification in Kenya refers to compliance with a set of principles and guidelines that ensure the quality and integrity of non-clinical laboratory studies. These studies are often conducted for research and development in areas such as pharmaceuticals, chemicals, and other fields where laboratory testing is crucial.
The GLP standards are established by regulatory authorities, such as the U.S. Food and Drug Administration (FDA) in the United States, the European Medicines Agency (EMA) in Europe, and similar agencies in other regions. GLP aims to promote the generation of high-quality and reliable data from laboratory studies, ensuring that the results are accurate, traceable, and can be independently verified.
