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A pharmaceutical and oncology research executive with more than 30 years of experience in drug discovery, angiogenesis and preclinical development. Dr. Brandt has advanced more than 50 compounds to clinical studies and brings deep expertise in pharmacology, cell biology, animal model development, GLP compliance and translational research.

A German physician and consultant with more than 25 years of independent experience in clinical pharmacology and drug safety, following senior international roles at Sandoz and Sanofi. He supports early clinical development, regulatory submissions and safety oversight across a wide range of therapeutic areas.

An experienced scientific writer with a strong background in pharmaceutical quality assurance and drug analysis. Since joining vivoPharm in 2006, Rosemary has specialised in preparing detailed preclinical study reports and brings practical GLP laboratory experience to every programme.

A quality assurance and preclinical research professional with more than 15 years of experience in toxicology, pharmacology, efficacy testing and GLP compliance. Her work spans regulatory compliance, study audits, SOP implementation and research staff training.

A research and development professional with more than 18 years of experience in preclinical research, translational science and early-phase clinical development. Dr. Kumar leads work in neuroprotective therapeutics, advanced pharmacokinetics and bioanalytical method validation.