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Medicilon’s Chemistry department has more than 100 chemists, who are experienced in the cooperation with major domestic and international pharmaceutical and biotech companies. Our services cover a variety of research interests in novel drug research, including target validation, hits evaluation, lead optimization, candidate nomination, pre-clinical development and IND filing.
As a global leader in chemistry services, we have a strong synthetic chemistry team with solid analytical chemistry support. We are committed to provide high quality products and services in a timely manner. With professional trainings, close communication and strong problem-solving abilities, our team could ensure projects progress is going smoothly.
Medicilon is a comprehensive CRO in the field of biology and medicine. We commit to provide integrated and efficient service. Our unique “tailored” process development mode also fully embodies this idea. We can collaborate with the clients to get target compound as soon as possible.
Chemical Analytical Center of Medicilon provides general analysis and purification services for the clients. Our experts have rich experience and proficient skills to solve problems. We are highly appreciated by the clients.
With a very small quantity of active pharmaceutical ingredients (API) or druggable candidate molecules, Medicilon’s pre-formulation service can provide valuable information and expertise to guide the compounds to next steps. Our pre-formulation team has extensive experience on handling a wide range of compounds and we can suggest the path forward for early success.
Medicilon provides full range of analytical services, including method development and validation, analytical testing and release, stability study, large scale separation and regulatory CMC documentation services. State-of-the-art instruments, cutting-edge technologies and experienced scientific staff ensure efficient, high-quality and cost-effective services.
Different dosage forms and manufacturing process may face different situations and problems in product development. A proper formulation and process should be employed to make sure the formulation and the scaled up process are reasonable and dependable and all the in process steps could be controlled effectively.
Our CMC department focuses on establishing large-scale synthetic routes along with formulation development and quality control. Our drug categories can be proprietary drugs or generic drugs. All studies are complied with ICH and CFDA guidelines.