Mark Lostrom

Supporting Regulatory Consultant

Mark Lostrom has over 40 years of experience in small and multi-national biopharmaceutical companies. Positions include research, development and multiple executive roles, including President and CEO. For the past 18 years he has provided consulting support exclusively in product development and regulatory affairs. Mark has managed and provided regulatory support for a wide range of therapeutic products from Phase I through NDA/BLA. He holds a bachelor’s degree in biochemistry from UCLA, a master’s degree in microbiology/immunology from Washington State University and U.S. FDA Regulatory Affairs Certification.