CDMO business mainly refers to providing customers with process research and development, process optimization, quality and stability research, customized production and other services of pharmaceutical intermediates and apis.
From the perspective of drug life cycle, the company mainly serves the clinical development stage of innovative drugs of multinational pharmaceutical companies and the commercial sales stage after the drug market, and also partly serves the research and development and marketing stage of generic drugs.
In the clinical trial phase and marketing application process of new drugs, the company provides customers with the process design, process amplification and optimization, chemical structure or component confirmation, quality and stability research, impurity research and other services of key intermediates for new drugs, and undertakes the small and medium-sized production of key intermediates in the process of research and development.
After drugs are approved for market and enter the commercial production stage, the company provides customers with large-scale production of key intermediates and continuous process optimization services to continuously improve and upgrade drug quality, production safety, EHS compliance and other aspects, effectively reduce costs and enhance product competitiveness.
Pharmaceutical process development optimization and industrial application