Ryan D. Foringer
Director of Regulatory Affairs Global Regulatory
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Overview
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Experience
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Credentials
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Insights and events
Ryan Foringer assists clients with U.S. Food and Drug Administration (FDA) regulations and policies focused on medical device technology. He leverages his training as an engineer and his combination of FDA and private sector experience to develop regulatory strategies and advise clients on medical device matters.
Ryan spent nearly four years at the FDA serving as a consumer safety officer, chemical engineer, and lead reviewer evaluating the safety of regulated products. He took his FDA experience to the private sector where he served as senior director of regulatory operations focusing on regulatory and clinical development of neurological, cardiovascular, and diabetes medical devices in a start-up environment. In this role, he led an international, interdisciplinary team in the preparation of FDA regulatory submissions while also advising affiliates on regulatory matters and compliance.
Ryan’s technical background, private sector experience, and training as a medical device reviewer at the FDA, give him a well-rounded perspective that he brings to clients as they navigate the FDA regulatory process.
Credentials
- B.S. Chemical Engineering, Rochester Institute of Technology, High Honors, 2013