Analysis of Pharmaceuticals’ Impurity - Regulations and Analysis for Carcinogenic Substances -
Příručky | 2020 | ShimadzuInstrumentace
GC/MSD, GC/MS/MS, HeadSpace, GC/SQ, GC/QQQ, LC/TOF, LC/HRMS, LC/MS, LC/MS/MS, LC/QQQ
ZaměřeníFarmaceutická analýza
VýrobceShimadzu
Klíčová slovandma, ndea, carcinogenic, substances, mutagenic, mms, ems, impurity, mode, ims, drug, mutagenicity, olmesartan, ndba, pharmaceuticals, ndipa, ebs, valsartan, acceptable, regulations, pharmaceutical, headspace, area, manufacturing, fda, api, mts, ttc, addition, analysis, velocity, neipa, instrument, ionization, ranitidine, mutagen, temp, limit, ibs, zhejiang, bms, substance, ratio, recovery, formations, note, nitrosamines, mbs, international, injection
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