Jacqueline Hanna, M. Eng.

Jacqueline Hanna

Associate, Regulatory Affairs
Background

With over 3 years of professional experience in medical device research and development, Jackie Hanna is a Regulatory Affairs Associate at MCRA.  As an associate, Jackie specializes in writing and reviewing regulatory submissions and developing regulatory strategy for clients.

Education

Jackie holds a Master of Engineering in Biomedical Engineering from Clemson University, as well as a Bachelor of Science in Biomedical Engineering from Clemson University with a focus on biomaterials and orthopedic products. She also holds an MBA Certificate in Technology Entrepreneurship.

Experience

Jackie Hanna is responsible for the development of regulatory submissions, including 510(k)s, De Novos, IDEs, Breakthrough Device Requests, and PMAs for clients. She supports regulatory strategy and analysis, as well as the design and review of pre-clinical testing.

Overview

Jackie Hanna supports regulatory strategy and submissions for the MCRA Regulatory Affairs department with a specialization in spine and orthopedics.

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