Jeannie Cecka

Jeannie Cecka is an experienced professional in the medical devices sector, serving as Principal Consultant at Cecka Consulting Group since May 2002, and as Clinical and Regulatory Consultant for glaucoma surgical devices at Santen since 2015. Previously, Jeannie held the position of Vice President for Regulatory and Clinical Affairs at Sunrise Technologies, where responsibilities included developing regulatory strategies for a pioneering Class III laser. At Baxter Healthcare, Jeannie managed worldwide clinical trials for the Novacor Division's LVAS artificial heart, while at Allergan, oversight of US and European clinical trials for ophthalmic surgical products was provided, leading to successful FDA submissions. Jeannie holds a Bachelor of Science in Biology from UC Irvine and an MBA from Pepperdine Graziadio Business School.