Seth J. Goldenberg, PhD

With over 20 years of experience in the MedTech industry, I am passionate about helping medical device and diagnostic companies achieve their clinical, quality, regulatory, and commercialization goals. As the President, Veeva MedTech I lead the customer engagement, market adoption, and product development strategy for Veeva Vault, a cloud-based platform that streamlines and simplifies the complex processes and data management across the product lifecycle.

My background in pharmacology, biomedical engineering, and regulatory affairs enables me to understand the challenges and opportunities facing MedTech innovators and to deliver solutions that meet their needs and expectations. I have supported hundreds of MedTech companies from inception through commercialization and post-market activities; have done this through my experience at the FDA, as a director of product development strategy at NAMSA, and as a consultant. I also play an active role in the industry, as a member of the Regulatory Affairs Professionals Society (RAPS), board member at the Medical Device Innovation Consortium (MDIC), and others. I am always eager to learn, collaborate, and share my insights and expertise with the MedTech community.