Trump Administration Executive Order (EO) Tracker
David Schreiber
Regulatory Specialist Global Regulatory
Languages
English, Hebrew, French
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Overview
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Experience
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Credentials
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Insights and events
David Schreiber assists medical device clients with regulatory matters. He leverages more than a decade of life science experience to support medical device clients with FDA submissions. At Hogan Lovells, David has been involved with FDA submissions across a wide range of device types, contributing to valuable experience in this field.
A critical reviewer, David loves to dive into a project, familiarize himself with new concepts and provide valued, content-related feedback, while paying great attention to details. David is CRA-qualified and familiar with regulatory and practical aspects of clinical study design and management.
Prior to joining Hogan Lovells, David was a Senior Life-Science Grant Consultant at the FreeMind Group. As a grant consultant, David specialized in obtaining non-dilutive funding for clients through U.S. federal agencies (National Institutes of Health, United States Department of Defense, and others). Taking a strategic, funding agency-oriented approach, David managed over 50 major multi-team international grant projects across all areas of medical device and drug development, and secured millions of dollars in project funding for his clients.
David is fluent in multiple languages including English, Hebrew, French, and Dutch, and is proficient in German. This often helps him in better connecting with European and Israeli clients.
Credentials
Education
- M.Sc., The Weizmann Institute of Science, 2016