2025 China Pharmaceutical CDMO Industry Insight Blue Book-Whitepapers

Home
Newsroom
classification

2025 China Pharmaceutical CDMO Industry Insight Blue Book

On April 30, 2024, Sapalizumab's new commercial production facility has officially obtained approval from the National Medical Products Administration (NMPA) of China. This marks the initiation of the commercialization process supported by Chime Biologics to assist clients in obtaining approval for their drugs to enter the market. Currently, Chime Biologics has 12 late-stage projects in progress.


We use cookies to understand how our audience uses our site.
Intellective Bio websites use cookies to deliver and improve the website experience.See our cookie policy for further details on how we use cookies and how to change your cookie settings Cookie policy.
Accept
Reject