Erdie De Peralta is Vice President of Clinical and Regulatory Affairs at Artio Medical. He is an experienced medical device professional with nearly 20 years of expertise in clinical and regulatory affairs, product development, and field and sales training.
Previously, Erdie was the Vice President of Regulatory and Clinical Affairs at ExThera Medical Corporation, where he led the company in the development and execution of regulatory and clinical strategies, including interactions with the FDA and other regulatory agencies. Prior to ExThera, Erdie held various regulatory leadership positions at OptiScan Biomedical, Abbott, St. Jude Medical, Boston Scientific, and Guidant Corporation. He has experience with implantable cardiac rhythm devices, PCI optimization, mechanical circulatory support devices, glucose monitoring systems, and hemofiltration devices.
Erdie has a Master’s degree in Nursing from New York University in New York, NY.
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