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On September 15th, 2023, the company was issued a Drug Manufacturing License, demonstrating that the company has established a comprehensive quality assurance system capable of ensuring production and quality management activities in accordance with the current Good Manufacturing Practice (cGMP) regulations in China.

On August 17th to 18th, 2023, ZheJiang Medical Products Administration conducted an on-site inspection of the company's application for a Drug Manufacturing License. The inspection results generally meet the requirements and are approved.