Daniel Trepanier

Over 25 years in the pharmaceutical industry. Experienced in pharmaceutical development including drug discovery, analytical and bioanalytical method development and analysis, preclinical pharmacokinetic, toxicological and  toxicokinetic studies, formulation development, drug manufacturing and  preclinical/clinical supply, preparation of preclinical regulatory submissions, interfacing with contract research organizations and patent attorneys. Real world experience in all aspects of drug development required to successfully move a drug from discovery, through myriad regulatory agency required studies, to Clinical Phase I/II status.