Good Laboratory Practice (GLP) is a system, which has been evolved by Organization for Economic Co-operation and Development (OECD) used for establishing non-hazardous nature of company products wherein the laboratory studies are planned, performed, monitored, recorded and reported.
GLP practices are intended to promote the quality and validity of test data.
GLP are the systems required to be adapted in development, quality control, quality system covering the manufacture and testing of medical therapies & drugs including active pharmaceutical ingredients, diagnostics, pharmaceutical products, and medical devices.
Because we keep the entire process hassle-free, GLP Certification can take just 7 - 30 days to complete based on your company's size. In fact, our 'Keep it simple' approach means we can: