What is GMP

"Good Manufacturing Practice" (GMP for short), is the global pharmaceutical industry *** with the observance of the quality management system, is the pharmaceutical production enterprises to enter the world's large market pass, is China's implementation of the core of the market access system for pharmaceutical enterprises. The current GMP was revised and implemented in 1998, the state through the full implementation, vigorously implement the GMP certification work, will make the level of drug production steadily improve, the quality of drugs under strict control.

The so-called GMP refers to a complete set of management system to ensure the quality of drugs from the quality of the personnel responsible for guiding the quality control of drug production and the quality of the production operators to the production plant, facilities, buildings, equipment, warehouses, the production process, quality management, process hygiene, packaging materials and labeling, up to the finished product of the storage and sale of the management system to ensure the quality of drugs. In short, the purpose of GMP is to prevent mixed batches, mixing, contamination and cross-contamination in the production of drugs to ensure the quality of drugs.

So, the implementation of GMP system for drugs is a means of state supervision and inspection of drug manufacturers, is an important element of drug supervision and management, but also to ensure the quality of drugs is a scientific and advanced management methods.