Dr. Jude Nwokike brings over 20 years of distinguished leadership in medical products development, quality assurance, regulatory systems strengthening, and pharmaceutical systems. As VP at USP he has led several global initiatives to ensure the quality and safety of medicines and spearheaded efforts to enhance the adoption of manufacturing standards and regulatory frameworks across nearly 60 countries, overcoming bottlenecks to accelerate access to life-saving medicines and vaccines. Before joining USP, Dr. Nwokike served as the U.S. FDA liaison to the Center for Drug Evaluation and Research, supporting the U.S. President’s Emergency Plan for AIDS Relief (PEPFAR) antiretroviral drugs program.