MANAGEMENT

Dr. Stagg has over 40 years professional experience in the medical product industry developing and obtaining US and International regulatory approvals to market medical products for biologics, pharmaceuticals and medical devices. He has worked for both large companies (Becton Dickinson and Allergan), start-up companies (AiViva BioPharma, Evolus and others) as well as providing scientific and regulatory consulting to multiple domestic and international companies. He is a member of  the Board of Directors for NOTOGEN, a company developing biologic products.

In addition to working with medical product companies, Dr. Stagg has been a leader in providing professional development programs in regulatory affairs as a cofounder chairman/president of the North Carolina Regulatory Affairs Forum, Orange County Regulatory Affairs Discussion Group, President of the Southern California pharmaceutical Discussion Group. From 2008 to 2021, he lectured on Pharmaceutical Regulations, in the UCI Continuing Education Program, University of California Irvine, Irvine, CA

Dr. Stagg also was the Industry Representative, FDA/Industry Regulatory Grassroots Partnership and in 1998 he received the FDA Commissioner’s Special Citation “For outstanding leadership and commitment in furthering FDA’s efforts to provide the consumer and the regulated industry with a more responsive Agency.” He was a Co-Chairman, US-Sub Technical Advisory Group (AAMI), and an US Representative to the International Standards Organization developing ISO 10-993, Biological Evaluation of Medical Devices. He is also involved in local community programs and has served on the Board of Directors, Discovery Science Center, Santa Ana, CA, since 2003.