What Does Rachel Sherman Think About Top FDA Regulatory Issues?

Speaking at the BIO CEO & Investor Conference, US agency's No. 2 official talks about compassionate use, opioids, clinical trial design, and the agency's succession plan.

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BIO CEO James Greenwood and FDA's Rachel Sherman at BIO CEO & Investor Conference • Source: Photo by Brenda Sandburg

Rachel Sherman, FDA's principal deputy commissioner, shared her thoughts on a variety of issues during a "fireside chat" at the BIO CEO & Investor Conference in New York Feb. 13.

During the Q&A session, Biotechnology Innovation Organization President and CEO James Greenwood asked Sherman about right-to-try legislation, FDA's ability to process applications of non-opioid pain products, the agency's plan to...

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