CH
01.Preclinical
02.Clinical Phase 1
03.Clinical Phase 2
04.Clinical Phase 3
05.Registration
06.Commercialization
Customized R & D and production of small molecules
Technology Development
Design & Screening of Synthetic Routes
Preparation of Preclinical Samples (Intermediates & API)
Development of Analytical Methods
Quality Research & Impurity Research
Process optimization
Continuous optimization of the synthesis process
Process safety assessment
Production of clinical samples under cGMP system
Optimization of analysis method
CDMO services
from PCC stage to commercialization, one-stop customized R & D and production services for small molecules
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