Medicilon Inc. Massachusetts

Medicilon Passes FDA Inspection, Reinforcing Global R&D Excellence

Strategic Validation of Global R&D Impact

This is Medicilon's first on-site FDA inspection in seven years, and the successful outcome significantly enhances its regulatory credibility. The milestone is a strong endorsement of its strategic vision, rooted in being "Innovation Driven, Quality Focused."

By the end of 2024, Medicilon has helped 520 INDs enter clinical trials, through the approval of China's NMPA, the US FDA, the EU EMA, the Australian TGA and the South Korean's KFDA.  These INDs include innovative drugs in various fields, such as 34 antibodies, 28 ADC drugs, 8 GLP-1 drugs, 6 PROTAC drugs, 3 botanical drugs, etc. Looking ahead, Medicilon will remain committed to increasing investment in technological innovation and R&D, and is committed to launching more innovative and more high-quality technology and service solutions, embracing the broad opportunities and challenges of the global pharmaceutical market, and promoting the development of the global pharmaceutical industry!

About Medicilon

From its inception in 2004, Shanghai Medicilon Inc. (stock code: 688202.SH) has been committed to providing comprehensive R&D services to pharmaceutical companies, research institutions, and any organizations working in the preclinical space. By the end of 2024, Medicilon has provided drug development services to over 2,000 clients worldwide, and has been involved in the research and development of 520 new drugs and generic drug projects that have been approved for clinical trials with IND applications.

View original content:https://www.prnewswire.co.uk/news-releases/medicilon-passes-fda-inspection-reinforcing-global-rd-excellence-302468239.html