Dawn Balazs-Metz, PhD

PRINCIPAL REGULATORY CONSULTANT

Dawn Balazs-Metz is a Switzerland-based regulatory affairs professional with over 20 years of medical device industry experience, offering a unique blend of expertise in product development, regulatory strategy, quality management, and design assurance. Dawn offers a bridge from EU and U.S. medtech markets to simplify complexity.

She has supported products from early concept through global commercialization across multiple device risk classes and development pathways, with core experience in vascular interventional and orthopedic implant sectors, where she led global market authorization efforts and partnered with major industry stakeholders. Her broad experience also includes active medical devices, digital health, drug delivery systems, combination products, cardiovascular and orthopedic implants, and medical device software. Driven by curiosity and continuous learning, Dawn provides clear, strategic, and impactful regulatory support that helps organizations bring safe, effective, and innovative medical technologies to patients worldwide. 

For more information, please see her LinkedIn Profile.