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Speaker

Debra Webster, PhD

VICE PRESIDENT, REGULATORY AFFAIRS, BLUEROCK THERAPEUTICS
Cambridge, Massachusetts, United States
Debra Aub Webster has over 25 years of experience in pharmaceutical research and the regulatory environment. She has started her regulatory career with the US FDA as Reviewing Toxicologist/Pharmacologist. As Vice President of Regulatory Affairs and Medical Writing, she leads projects for biologic and regenerative medicine product development programs. In this capacity, she provides guidance on clinical, nonclinical and regulatory aspects of strategic product development, author’s regulatory documents and acts as the Regulatory Representative in interactions with the FDA.
Speaking In
4:15 PM - 5:15 PM (PDT)
Wednesday, June 15
The number of cell and gene therapies entering clinical trials is growing at an increased rate…