Bhaswat Chakraborty

bioequivalence ct clinicaltrials drug discovery clinical clinical trials replicate design pharmacokinetics plasma proteins drugs clinical quality biosimilars pk pharmacovigilance corrective and preventive action root cause analysis outliers two period crossover respiratory pbpk mdi orally inhaled ivpt ivrt non=linear mrdfs fed studies parallel crossover complex generics gdufa ii primary objective pivotal medical devices clinical trial style grammar technical writing efficacy safety clinical pharmacology us fda bla nda newton inter-personal intra-personal adaptation bpharm mpharm five ways to stop plagiarism root cause anti-plagiarism softwares originality plagiarism risk based approaches data integrity bioethics clinical research pharmacy ethics pre-clinical. pharmacists development regulatory non-clinical biosimilar phase ii trials cancer acceptance limits confidence intervals drug-products data integrity fda patent exclusivity gcp glp india fda risk management career science average polpulation individual drug delivery system cancer ct phase ii go no go bayesian toxic signals nanotechnology