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Related News: DMF is the main management method for APIs in developed countries in Europe and the United States. Under the DMF system, API companies can submit DMF filing documents to the regulatory authority at any time, but the regulatory authority will not conduct technical reviews on them. When the drug is administered, the regulatory authority will associate and review the drug substance and the preparation.452-75-5 Their pharmacological activity plays a direct role in the diagnosis, cure, mitigation, treatment, or prevention of disease.2-bromo-6-fluoro-4-methylpyridine CAS:180608-37-1 As far as chemical raw materials are concerned, China occupies a large share in the field of bulk raw materials and has become one of the world’s largest suppliers of chemical raw materials.922727-92-2 As far as chemical raw materials are concerned, China occupies a large share in the field of bulk raw materials and has become one of the world’s largest suppliers of chemical raw materials.High-barrier generic drugs: Usually for the production of drugs whose patents have just expired or are about to expire, the market is only competed by original research and a few generic drug companies.
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(3,4-Dimethoxyphenyl)acetone Cas:776-99-8 | View Details |
Quinoxaline Cas:91-19-0 | View Details |
1-Fluoro-3,5-dimethylbenzene | View Details |