Shraddha More

Shraddha More is a Senior Staff Regulatory Affairs Specialist at Stryker Spine, bringing over 11 years of experience in executing regulatory strategies for Class II and III medical devices across global markets, including the EU, Canada, Asia, the Middle East, and Russia. Shraddha has authored numerous regulatory submissions, including fourteen 510(k)s and multiple MDD and MDR applications, while also mentoring emerging professionals in regulatory affairs. Previously, Shraddha held positions at various organizations, developing comprehensive quality management systems and leading successful audits. Educationally, Shraddha holds a Master's in Regulatory Affairs and a Master's in Pharmacy, both with high GPA distinctions.