CRO
1970-01-01 08:00:00
Detailed introduction
1, undertake different types of raw materials and formulations of the establishment and validation of analytical methods
2, to undertake the API test lab to pilot scale synthesis process development, optimization, change and process validation
3, to undertake the comparative study of the mass spectrum of the drug substance and the preparation of the complex mass spectrum and the reference preparation
4, to undertake the research on the prescription variables and the parameters of the preparation process variables, to ensure that the consistency of generic drugs and reference formulations in vitro dissolution
5, synthetic technology industrialization
6, to undertake the change of prescription, preparation process supplement application, and the original preparation of the dissolution test in vitro and other comprehensive technical research work