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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-(2-Tetrahydrofuroyl)piperazine hydrobromide 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.1-bromo-2,3,4,5,6-pentafluorobenceno CAS:344-04-7 The move could force international drugmakers to further cut prices and enable copycat medicines to replace imported off-patent brands at faster pace.Diclorodifenilsilano CAS:80-10-4 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.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.
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Titanium tetraisopropanolate Cas:546-68-9 | View Details |
1-Phenyl-1-cyclopentanecarbonitrile | View Details |
5-(2-ETHOXYPHENYL)-1-METHYL-3-N-PROPYL-1,6-DIHYDRO-7H-PYRAZOLO[4,3-D]-7-PYRIMIDINONE Cas:139756-21-1 | View Details |