CRD,CRO, CMO & CDMO Services

As more candidates entering preclinical and clinical development stages in the pharmaceutical industry, demands for GMP-quality have soared. Changzhou Pharmaceutical Factory has designed and built excellent API manufacturing facilities and factories in accordance with the specifications of the United States and the European Union, enabling us to provide customized and flexible cGMP API manufacturing services to meet your research and production needs from R&D to clinical research, and support your drugs development.

Our GMP Services:

Flexible Production

Changzhou Pharmaceutical Factory has introduced the automated equipments and tighten controlled CGMP production line for all kinds of APIs. Using our unique production line, we can complete the production of APIs products for clinical use according to specific requirements, and support the phase I-II clinical research trials drugs. We can provide research-grade, product design verification and validation, or GMP-compliant products assisting you from research to clinical phase I and II. 


Rigorous Analysis Process

According to customers' requirements for different products,Changzhou Pharmaceutical Factory can develop analysis methods of product purity, related substances, elemental impurities, residual solvents, content, microbial limit etc.. Changzhou Pharmaceutical Factory performs methodological validation of the developed analytical methods to ensure that they truly meet nucleotide and drug detection and quality control requirements.

Quality And Risk Management

Changzhou Pharmaceutical Factory uses quality management tools to help customers establish a complete whole-process quality management system. At the same time, we use a risk management system to help customers control the risks of drug development processes.