Celina Abi-Khalil, Ph.D. has extensive experience in regulatory affairs and healthcare industry. Celina has worked as a Clinical and Regulatory Affairs Manager at Wyss Center for Bio and Neuroengineering, held positions at Guerbet, Alispharm, and academic institutions, and has a strong educational background with a Ph.D. in Microbiology and Immunology. Their expertise lies in defining regulatory strategies for medical devices, managing interactions with regulatory bodies, and overseeing international registrations and sales authorizations.
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