9-bromo-10-(4-phenylnaphthyl-1-yl)anthracene

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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.34486-06-1 At the same time, through years of imitation and advanced technology learning, more and more domestic companies have participated in the field of highly original and characteristic APIs.2-Fluoro-3-Chloro-5-Bromopyridine At the same time, through years of imitation and advanced technology learning, more and more domestic companies have participated in the field of highly original and characteristic APIs.Diethyl ((2-(6-amino-9H-purin-9-yl)ethoxy)methyl)phosphonate Since the listing of high-barrier generic drugs involves quickly bypassing or challenging process patents of original research products within a short period of time, API companies play an important role in the process of marketing and sales of generic drugs.In addition, although the API and intermediate industries are capital-intensive and technology-intensive industries, new competitors are still joining.