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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.1-Boc-2-[4-(2-pyridinyl)benzylidene]hydrazine The Company selected the top-performing clone for generation of the master engineered iPSC bank for GMP production of FT819.1-fluoro-10-clorodecano CAS:334-62-3 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.2-bromoacetofenona CAS:70-11-1 The Company has established a leadership position in the clinical development and manufacture of universal, off-the-shelf cell products using its proprietary induced pluripotent stem cell (iPSC) product platform.AstraZeneca Plc said on Monday that its cancer drug met the main goal of delaying the progression of a form of lung cancer.
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[1-(4-phenyl-1H-imidazol-2-yl)-ethyl]-carbamic acid benzyl ester | View Details |
2-Cyclohexylmandelic acid | View Details |
4-Chloro-2-methylbenzonitrile | View Details |