Dr Susan had the up-to–date clinical background knowledge together with a diverse wealth of knowledge and experience in advanced clinical epidemiology, clinical trials, evaluation of diagnostic test kits.

She has cumulative knowledge and hands-on experience in managing phase I – Phase IV Studies, Single center and multi-center studies, Investigator initiative and Pharmaceutical sponsored studies.

In addition, she has hands-on experience in scientific consultations on Pre-Investigational New Drug Application (Pre-IND) and regulatory submissions (HAS & FDA) as well as Scientific Rebuttal of regulatory submissions; and currently practicing as a medical consultant.