Sema Ariman

Sema Ariman is an experienced professional with a background in regulatory affairs. Sema started their career at Abbott Laboratories in 1999, where they held roles such as Senior Process Development Engineer and Manager of Operations Support. At Allergan, they served as a Senior Manager in both CMC Regulatory Affairs and as a Global Regulatory Lead, overseeing various projects in the Ophthalmology therapeutic area. Sema then joined SAGE Therapeutics as a Director of CMC Regulatory Affairs before moving on to their current position as the Executive Director of Global Regulatory Strategy at Sarepta Therapeutics. Throughout their career, Sema has demonstrated expertise in developing regulatory strategies, managing FDA submissions, and leading global regulatory teams.

Sema Ariman, RAC, has a Bachelor's Degree in Chemical Engineering from Northwestern University. Sema also completed the Regulatory and Quality Compliance Graduate Certificate Program at Purdue University in 2010. Additionally, Sema has obtained the US Regulatory Affairs Certification from RAPS in 2011 and the Certified Manager of Quality/Organizational Excellence certification from ASQ in 2006.