Dr. Haven McCall is a senior level regulatory affairs executive who has spent the last 18 years working in FDA regulated industries, specifically within Human Cells and Tissue-Based Products (HCT/P), medical devices and pharmaceuticals. Throughout his career, he has held various regulatory, quality and clinical research positions with global biotech companies.

Dr. McCall is an active member of the Regulatory Affairs Professionals Society (RAPS), The Organization for Professionals in Regulatory Affairs (TOPRA – Europe) and the American Society for Quality (ASQ) and he holds several professional certifications. His graduate studies at the University of Southern California focused on the improvement of quality in hospitals and enhancing the standard of care for patients through the application of risk management approaches.

Haven enjoys working with organizations to ensure they understand and comply with FDA regulations. He actively consults for doctors, start-ups and established organizations with the goal of educating, training and implementing quality systems that meet the expectations of the US FDA.