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PDA Webinar: Advancing Advanced Therapy Medicinal Products in a Dynamic Regulatory Environment

Jun 18, 2020
Eastern Standard Time | Online
  • Virtual
  • Conference
  • Online

Overview

Moderator: Michael N. Blackton, MBA, Vice President, Quality, Adaptimmune LLC 

Join us for an in-depth exploration of the current state of development and regulatory thought for the advancement of advanced therapy medicinal products globally.

This webinar will examine cell and gene therapy product development and innovation in a way that helps foster understanding of the evolving landscape of global regulatory requirements in order to advance these therapies through approval and beyond.

Following two presentations by leaders in the field, get your questions answered during a live 30-minute Q&A session with the speakers.

This webinar is presented as part of the 2020 PDA Advanced Therapy Medicinal Products Month.

Agenda

  • 11:00 a.m. – 11:30 a.m.
    Engineered T Cell Therapies: Development, Global Regulatory Approvals, and Future Trends
    Bruce L. Levine, PhD, CCI Deputy Director, Technology Innovation and Assessment,University of Pennsylvania

    11:30 a.m. – 12:00 p.m.
    Dennis Williams, PharmD, Senior Vice President, Late Stage Development, Adaptimmune LLC

    12:00 p.m. – 12:30 p.m.
    Q&A with Speakers

Highlighted Speakers

Bruce L. Levine
Bruce L. Levine
University of Pennsylvania
Dennis  Williams
Dennis Williams
Adaptimmune LLC

Registration Fees

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Registration Type Price
Member $200
Non-member $200
Gov't/Health Auth./Academic $200

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