Jayesh Rajput

pharmacy pharmaceutical science drug diseases delivery quality control system respiratory disease corona regulatory chromatography development techniques clinical trial pharmacist related coronavirus electrophoresis modern pharmaceutics covid-19 glenmark qa dept industry pharmaceutical analysis statistics silicosis immunological assays trials biostatics protocol bioassay affairs reference quality assuarance management industrial quality education europe fda ich ectd ctd liasion regulations m pharm regulatory affairs post approval cmc pharma systems vaccine assays bioluminescent assay elisa microbiology pharmacology silica silica dust manufacture virus training pharma industry mucosa healthcare hyphenates technique flash institutions authorities status patent patenting herbal medicine oath principle applications blotting concepts basic chroma case study electronics radioimmunoassay immunoassay radio immunoassay cgmp pq oq iq dq urs types of validation types of calibration ich and who guidelines for calibration master plan scope and merits of validation pharmaceutical validation bioelectronic medicines 3d printing of pharmaceuticals customized drug delivery telepharmacy pharmacogenomics pharmacogenetics personalized medicine polymers controlled release dosage form sustained release dosage form dry granulation roller compactor pharma roll compactor roll compactor anova chi square dissolution parameters diffusion parameters study of consolidation parameters solubility compaction profiles distribution of forces effects of friction consolidation compression physics of tablet compression compression and compaction optimization preformulation concepts total quality management layout of buildings regulatory requireents for product approval cro (contract research organisation) post marketing surveillance in-vivo scale up process approval changes be and drug product assessment nda approval process in vitro anda regulatory approval process drug product performance cfr (code of federal regulation) hatch waxman act generic drugs product development distribution records dmf (drug master file) master formula record (mfr) documentation in pharmaceutical industry pharmaceutics transdermal ocular ocular drug delivery system row tga mhra industrial management iso electric focusing electrophoresis moving boundary electrophoresis zone electrophoresis capillary electrophoresis gel electrophoresis paper electrophoresis paper chromatography thin layer chromatography ion methods of formulation and its evaluations mechanism of drug permeation advantages and disadvantages of grdds principle of muco adhesion buccal drug delivery systems modulation of gi transit time approaches to extend gi transit principles concepts gastro retentive drug delivery system thank you anda for generic drug ways and means of us registr novel therapies obtaining nda biologics api