Over careers that average well over 25 years each in drug discovery and development within both Pharma, CRO and consulting sectors, the RDS consultants have been involved in most aspects of preclinical and clinical pharmacokinetics, drug metabolism and ADME studies from both logistic and strategic perspectives. This experience includes technical lab supervision, external study design, placement and monitoring, pharmacokinetic/ toxicokinetic data calculation and analysis, as well as preparation of project reports, regulatory documents (IND, NDA, package inserts), position papers, and literature summaries. In addition, they have published and presented widely in the areas of animal and human ADME, drug metabolism and drug interactions, pharmaceutical technology, pharmacokinetics and clinical research, medicinal chemistry, radiolabeled synthesis and bioanalysis.
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