JayeshRajput7

pharmacy drug diseases science pharmaceutical delivery regulatory system quality control respiratory disease corona modern pharmaceutics clinical trial development electrophoresis related techniques pharmacist chromatography coronavirus covid-19 glenmark qa dept industry silicosis statistics pharmaceutical analysis 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 industrial management 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 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 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 europe fda ich ectd ctd liasion regulations m pharm regulatory affairs post approval cmc pharma systems vaccine assays bioluminescent assay elisa radio immunoassay immunological assays trials protocol affairs quality assuarance quality education industrial management reference bioassay biostatics immunoassay radioimmunoassay electronics case study chroma basic concepts blotting applications principle oath medicine herbal patenting patent status authorities institutions flash technique hyphenates healthcare mucosa pharma industry training virus manufacture silica dust silica pharmacology microbiology