Swapnil Fernandes

india us fda quality assessment biologics licensing approval europe user experience marketing authorisation vaccines regulatory submissions regulatory affairs ectd ich common technical document ctd recommended dietary allowance fssai nutraceuticals manufacture import nutrccaeuticals nutraceuticals fssai rda drug manufacturing practices pharmaceutical quality us good manufacturing practices manufacturing practices current gmp cgmp 510(k) medical devices label us medical device labelling regulations us medical device regulations medical device qms medical device labeliing quality management system us medical device labeling requirements 21 cfr part 801 21 cfr part 820 us drug regulations us fda regulations fda code of federal regulations cfr pharmacy council of india pci drug regulations pharmacy act 1948 pharmacy act pharmaceuticals pharmacy indian pharmacy rules automation in glp glp galp