Marina ICHÉ is a recognized expert in clinical and regulatory development strategy, specialized in oncology and early-stage development. With nearly 30 years of experience in the pharmaceutical and biotechnology industry, and as the founder of ILife Consulting, Marina advises biotech executives in France and Europe, providing her expertise on regulatory affairs, clinical operations, quality assurance and fundraising.
Her background includes managing complex international projects, regulatory submissions to agencies (FDA, EMA) and supervising clinical trials for numerous oncology indications in pharma as well as in various biotechnology companies. Before founding ILife Consulting, Marina led the clinical evaluation and development of a portfolio of biotechnology companies for a private fund, supervising Clinical Operations, Regulatory Affairs and Quality Assurance of the companies within this fund.