Earnestly study the 2010 version of GMP to further improve the quality management level

The 2010 version of "Good Manufacturing Practice for Drugs" (GMP) has been officially implemented since March 1, 2011. The implementation of the new version of GMP is a general trend for Chinese pharmaceutical manufacturers to comply with global drug regulatory regulations and technical standards and continue to move towards unification. It is a concrete manifestation of the spirit of being highly responsible for the safety and effectiveness of people's drug use, and it is the need for drug supervision and management departments to improve their supervision and management level, it is a good thing for the country, the people and the enterprise.

The implementation of the new version of GMP is a systematic project, the implementation process is very complex. In order to successfully complete the GMP renewal and relocation of the new factory building in 2013, the company decided to arrange comprehensive training for employees at all levels from November to systematically learn the new version of GMP. Learning will be carried out from point to surface, from shallow to deep, and the final examination results will be included in the performance appraisal. At present, the first stage of training and learning for middle-level cadres has been completed, with excellent examination results and satisfactory training results.

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