Wei Li Zhibo quality is life, and has established a quality management system that covers the research and development of the drug production. On the basis of the US GMP, the mid-test production base is referred to the relevant law of the US FDA and EU EDQM.
The principles of regulations and guidelines, formulate a complete production quality management system and strictly enforce it.
Viti Li Zhibo has established a comprehensive antibody drug process development, mid-test production (500L scale) and quality testing platform, can also meet the clinical trial application of China NMPA and US FDA and 1-2 clinical trials.
Preparation of samples.
Viti Li Zhibo has established a comprehensive antibody drug process development, mid-test production (500L scale) and quality testing platform, can also meet the clinical trial application of China NMPA and US FDA and 1-2 clinical trials.
Preparation of samples.
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