Michael Coladonato has over 6 years of experience in US and Global regulatory affairs for spine and orthopedic devices. Michael specializes in regulatory strategy, writing of regulatory submissions, analysis of pre-clinical and clinical data, development and execution of systematic literature searches, and drafting and reviewing of Clinical Evaluation Reports.
Michael Coladonato received his Bachelor’s in Biomedical Engineering from Catholic University of America.
Overview
As a manager of regulatory affairs, Michael manages and supports various US and EU projects in the spine and orthopedic therapeutic area.