Mi Mandy is the Head of Regulatory Affairs at EC Pro Acute Care, with extensive experience in regulatory strategies across MDSAP countries, US FDA submissions, and EU registrations. Previously, Mi managed regulatory affairs at Siemens Healthineers and Philips, focusing on high-risk medical devices and ensuring compliance with global regulations. Mi holds a Bachelor's degree in Pharmaceutical Engineering and a Master's degree in Pharmaceutical Sciences, both from Sichuan University. Known for strong communication skills and the ability to collaborate effectively with diverse teams, Mi has successfully led numerous product registration projects and established quality management systems.
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