Robert A. Herrmann is currently the Director of Neurointerventional Regulatory Affairs at MCRA, LLC, where they leverage over 20 years of experience in the medical device field to assist companies in bringing their devices to market. With a strong focus on innovation and detail, Robert has significant expertise in regulatory affairs, product development, and medical device quality systems, including extensive FDA experience. Their background includes roles such as Vice President of Engineering at eVasc Medical Systems and Engineering Manager at Angiotech Pharmaceuticals, where they contributed to multiple patent applications and product innovations. Robert earned a PhD in Biomedical Engineering from Duke University and a BS in Chemical Engineering from the University of Virginia.
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