Suraj Pamadi

jss medical medical device device regulatory affairs regulation registration classification suraj phase1 format pharmacy phase2 phase3 phase4 phase0 jss. research biomedical icmr trial clinical new drug application investigation guidance pharmaceutical copp certificate product compensation for participation confidentiality submission of application ethical review procedures guildlines ethical human subjects functions definiton examples labelling import flow chart india marketing notified heart stents coronary stents coronary overview market authorization cfr cardiac hde hud stent agent 510(k) approcal substantial equivalent process iii i type ii 510k industry. indian