Md. Zakaria Faruki

gmp medicine pharmaceutical healthcare who pharmaceuticals quality efficacy safety regulatory pharmacovigilance qms pharmaceutical industry pharmacist career training industry gdp ich efficacy and safety drug development physician focal point adverse drug reaction suspected adverse event psur adverse event legislation regulatory authority fda dgda medicines glp tqm personnel marketing authorization profession pharmacy knowledge skill organization corporate quality assurance product development sop pharmaceutical products process validation guideline accident prevention workshop human resources manpower health recall customer complain product gdocp) document record cgmp test product reference product biowaiver drug biosimilarity bioequivalence usfda pharmaceutical product nda good clinical practice products stability adverse drug event adverse drug reactions. post-marketing surveillance drug safety clinical studies ectd