Products have a wide array of sensitized risks during the many processes involved in manufacturing. GMP primarily aims to eliminate these risks at every stage of production. The end product cannot always be effectively verified after the entire manufacturing process is complete. Many hazards such as mislabeling of drugs or variations in the composition of basic ingredients can cause massive harm to end-users and are perhaps one of the worst forms of “prescribed threats”.
In short, GMP assures that manufactured products meet their promised quality standards with minimal deviations. In fact, GMP has proved highly effective in managing large scale drug manufacturing units by conducting regular audits.