AN Ce

AN Ce is a regulatory professional with over 11 years of experience in the Medical Device and Pharmaceutical industries, including 8+ years focused on Global Regulatory Strategy. They have successfully developed and executed regulatory strategies for high-risk medical devices under EU MDR, FDA, and global frameworks, achieving timely approvals across multiple markets, including the US, EU, and China. AN Ce has held roles with Philips and GE Healthcare, where they managed regulatory compliance and strategy, resulting in significant business value and enhanced patient safety. With educational credentials including a Bachelor's degree in International Trade and Economy and a Master's degree in Pharmaceutical Control and Supervision, AN Ce is passionate about regulatory excellence and compliant innovation.