WuXi Biologics , a leading global Contract Research, Development, and Manufacturing Organization (CRDMO), announced that three of its manufacturing facilities in Wuxi – MFG1, MFG2, and DP5 – have received GMP certification from Türkiye İlaç ve Tıbbi Cihaz Kurumu (TITCK). This marks the first GMP inspection conducted by Turkey's TITCK at WuXi Biologics. Achieving the certification underscores the company's commitment to upholding stringent international quality standards across its global network.

WuXi Biologics has consistently demonstrated a proven track record of adherence to the industry's most rigorous quality standards. As of the end of June 2025, it has successfully passed 44 regulatory inspections, including 22 conducted by the FDA and the EMA. The company also holds an industry-leading achievement with a 100% pass rate for Pre-License Inspection (PLI) by the FDA. Additionally, WuXi Biologics has passed more than 1,700 GMP quality audits by global clients, including more than 200 audits by EU Qualified Persons. Currently, the company operates 16 GMP-certified drug substance and drug product facilities within its global network. Its world-class quality and compliance capabilities remain the cornerstone of clients' trust.

Dr. Chris Chen, CEO of WuXi Biologics, commented, "We are delighted to receive GMP certification from Turkey's TITCK—our first recognition in the Turkish market, and a clear sign of WuXi Biologics' capability to tap into emerging markets. With a deep understanding that quality is crucial to ensuring safety and efficacy in the global pharmaceutical industry, we are steadfast in upholding the highest standards across our entire network. Looking forward, WuXi Biologics will continue building on our first-class quality system and exceptional service capabilities, remaining dedicated to enabling our clients in bringing high-quality biologics to patients worldwide."