Principal Regulatory Affairs Specialist, Smith+Nephew

Miriam Wilcox is a seasoned professional with over 20 years of experience in the medical device industry. Her expertise spans regulatory affairs, quality engineering, and project management. She has spent a significant portion of her career working on implants, and device remediation to new and updated regulations.  Currently, her focus is on software medical devices, a rapidly evolving area of industry especially with the rise in scrutiny on AI derived devices. Miriam is known for her focus on collaboration with regulators and cross-functional teams.