Speaker Information
Meet the speaker and learn more about their expertise, experience, and contribution to advancing clinical research.
Pierre-Frederic Omnes
Independent Consultant,
Omnes Advisory
Pierre-Frédéric Omnes is an independent regulatory advisor and clinical trial regulatory leader with more than 20 years of experience in global regulatory operations, EU Clinical Trial Regulation (EU CTR), and the Clinical Trials Information System (CTIS). He advises biotechnology companies, pharmaceutical sponsors, and CROs on regulatory strategy, CTIS implementation, operational excellence, and global clinical trial execution. Pierre currently serves as one of three industry representatives on the European Medicines Agency (EMA) CTIS Taskforce and has been actively involved in the design, development, testing, and evolution of CTIS since 2016.
