“GLP is a formal regulation that was created by the FDA (the United States Food and drug administration) in 1978. They assure the quality & integrity of data submitted to FDA in support of the safety of regulated products”. In reference to the above statement, discuss in detail, the core principles of Good Laboratory Practices. (10 marks)

Answer rating: 100% (QA)

the core principles of Good Laboratory Practice The managerial quality control system covering the organisational process and the conditions under which nonclinical health and environmental studies ar... View the full answer