GCP is not only suitable for people who undertake clinical trials in different stages (I-IV) (including hospital administrators, members of ethics committees, experts, professors, doctors, pharmacists, nursing staff and laboratory technicians), but also suitable for drug supervision and management personnel, clinical researchers in pharmaceutical enterprises and related personnel. Standardize the behavior of relevant personnel.
Extended data
The "Quality Management Standard for Drug Clinical Trials" has been considered and adopted at the ministerial meeting of the US Food and Drug Administration on June 4, 2003, and is hereby promulgated. This specification shall come into force as of September 6, 2003.
In order to ensure that the clinical trial process of drugs is standardized, the results are scientific and reliable, the rights and interests of subjects are protected, and their safety is guaranteed, this specification is formulated according to the Drug Administration Law of People's Republic of China (PRC) and the Implementation Regulations of the Drug Administration Law of People's Republic of China (PRC), with reference to internationally recognized principles.
Baidu Encyclopedia-Quality Management Standard for Drug Clinical Trials