Jing Medicine's Next-Generation EGFR PROTAC Program Clears U.S. FDA for Clinical Trials | Backed by SDM
SDM Bioservices, serving as Jing Medicine’s regulatory strategy partner, played a pivotal role in the successful FDA application process. Leveraging deep expertise in global regulatory affairs, SDM delivered comprehensive GAP analysis, technical document preparation, and submission management services. SDM also supported Jing Medicine’s IND application in China, establishing a robust foundation for the program’s global development strategy.
 
                             
             
                             
                             
                             
                             
                             
                 
                 
                