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Ron has over 30 years’ experience as a clinical pharmacologist/toxicologist in the pharmaceutical and biotech industry. He has written the pharmacology/toxicology and clinical pharmacology sections for global regulatory submissions, including pre-IND packages, IND/CTA, BLA/NDA/MAA packages as well as investigator brochures and annual reports. Prior to consulting, he was in leadership roles at Arena, Takeda, J&J, Schering-Plough, Ligand, and Bayer.