guarantee every link of pharmaceutical production
Mature Manufacturing Capabilities
and System Protection
Tasly Biopharma has formulated a quality policy of “Compliance with Laws, Quality First, All Staff Participation, Continuous Improvement” in accordance with the “Good Manufacturing Practice for Pharmaceutical Products” (GMP) and “Pharmaceutical Administration Law” and established a scientific, systematic and effective quality management system by integrating international laws, regulations and guidelines. The company has formulated and implemented quality objectives that meet the requirements of the quality management system, and has systematically implemented the requirements of drug safety, effectiveness and quality control in the entire process of production, quality control, product release, delivery and post-marketing management of drugs, and continued to provide customers with products that meet the intended use and registration requirements.