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Monday, June 20 • 1:30pm - 2:30pm
#119: Is it Time to Change the Accelerated Approval Pathway?

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Component Type: Forum
Level: Intermediate
CE: ACPE 1.00 Knowledge UAN: 0286-0000-22-520-L04-P ; CME 1.00; RN 1.00

A discussion on potential changes to accelerated approval pathways to streamline processes while continuing to maintain the gold standard of approval.

Learning Objectives

Explain advantages of the accelerated approval pathway; Discuss future potential changes to accelerated approval pathways.


Khyati Roberts, RPh


Industry Perspective
Kristin Van Goor, PhD

Patient Perspective
Jeff Allen, PhD

avatar for Jeff Allen

Jeff Allen

President and Chief Executive Officer, Friends of Cancer Research, United States
Jeff Allen, Ph.D. serves as the President and CEO of Friends of Cancer Research (Friends). During the past 25 years, Friends has been instrumental in the creation and implementation of policies ensuring patients receive the best treatments in the fastest and safest way possible. As... Read More →
avatar for Kristin Van Goor

Kristin Van Goor

Regulatory Policy and Intelligence, Global Regulatory Affairs, Vertex Pharmaceuticals, Inc., United States
Kristin Van Goor received her Ph.D. in Genetics from Yale University and continued her research as a post-doctoral fellow in the Cancer Genetics Branch of the National Human Genome Research Institute at the NIH. She then spent a number of years at PhRMA as the Assistant Vice President... Read More →
avatar for Khyati Roberts

Khyati Roberts

Head US/Canada, Regulatory Policy and Intelligence, AbbVie, United States
Khyati Roberts leads regulatory policy advocacy efforts for U.S. and Canada and co-leads the day-to-day operations of the global regulatory policy and intelligence team at AbbVie. She has over 30 years of regulatory experience including nearly 14 years at the U.S. FDA/Center for Drug... Read More →

Monday June 20, 2022 1:30pm - 2:30pm CDT
Room 187 McCormick Place 2301 South Indiana Avenue Gate 40 Chicago, IL 60616
  09: Regulatory, Forum