Route development and large-scale production of intermediates
Screening of Synthetic Routes
Process development, optimization and scale-up
Quality research
Stability study
Design & Screening of Synthetic Routes
Preparation of Preclinical Samples (Intermediates & API)
Development of Analytical Methods
Quality Research & Impurity Research
Continuous optimization of the synthesis process
Process safety assessment
Production of clinical samples under cGMP system
Optimization of analysis method
complete DCS control
Intermediate & API production
Multiple and flexible business cooperation modes
Complete regulatory registration team
Route development and large-scale production of intermediates
Screening of Synthetic Routes
Process development, optimization and scale-up
Quality research
Stability study
Process development and optimization
Quality research
Study of impurities
Stability study
China, the United States and Europe registration declaration
API validation production
Production of cGMP APIs
Drug substance association of preparation
Registered variety
10, turn "A" 4
Registered variety
2
Registered variety
2
Milligram to kilogram products, as well as the preparation and separation of various impurities.
Provide complete mass spectrum, NMR and analysis
Development of preparation and purification production process, salt conversion, post-treatment of preparation liquid, etc.
500 L reaction system, pressurized 10 kg.
2000 L reaction system, 63 kg pressure.