Qyuns Therapeutics Co. Ltd. has announced that its subsidiary, Jiangsu Cellularforce Biopharma Co., Ltd., has successfully passed the EU Qualified Person (QP) audit and received the official compliance audit report. This achievement confirms that the company's industrialization base meets EU Good Manufacturing Practice (GMP) standards for pharmaceuticals. The audit, conducted by a senior QP in accordance with EudraLex Volume 4 and related guidelines, recognized Cellularforce's high-standard quality management system, advanced facilities, and professional capabilities. This milestone supports the company's efforts in providing globally compliant biologics CDMO services. No grant or funding involving multiple organizations was mentioned in the announcement.