New products are added every yearCompetitiveness - quality and cost of products. Entering the market in Europe. High productivity. CTD /DMF documentation on European and FD standards.
Our specialists are graduates of the best universities in China, America, Australia and Europe. Thanks to our extensive experience, the team conducts research and develops medicines of any complexity, quickly and efficiently. Speed is one of the main advantages of companies, so we can guarantee you the development of the drug in 4-8 months and the rapid transfer of technology to your production.
Based on ICH approaches, ISO standards, and GMP principles. Currently, the company has a large number of quality management system documents, as well as SOP. Provide systematic and standardized management of original project records, project registration data, and R&d team data.
