I will do pharmacokinetic analysis and adverse drug event reporting

With immense knowledge on Adverse Drug Reaction(ADR) monitoring and reporting,

patient care, prescription monitoring, drug interaction monitoring, FDA modules, eCTD submissions, ICH E6 & ICH E3 principles and Clinical Study Reports, I am Eager to work on any Phase involved Clinical Study reports and Protocols, where I could produce regulatory complaint one in accordance with GCP and GMP procedures with statistic analysis and dossier preparation in a hassle free and flawless manner.