2025<<<<><<<<< Expert Group On-site audit of the Jingjing pharmaceutical industry GMP. > as High Imitation of APIs, amino acids and vitamins High-tech Enterprise, with standardized quality system and efficient production management, successfully complete the inspection Work.

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During the period, Japan PMDAThe whole process of raw material production, Complent quality management system and normative production practices, showing solid compliance ability . JapanGMPCertification is known for its strictness, One of the core authority criteria, Japan and the global market lays the key foundation. Jingjing Pharmaceutical will follow up the audit results, continue to optimize quality management, enable products with innovative technologies and international standards, and accelerate the development of .