Regulatory Strategies for Gene Therapy Product Development, Upcoming Webinar Hosted by Xtalks

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In this free webinar, the featured speaker will give an overview of gene therapy product development and discuss how to navigate the regulatory landscape. Attendees will learn about overcoming hurdles from clinical trials, manufacturing and regulatory challenges as well as emerging regulatory requirements.

This is an exciting time in the industry with products being developed at an accelerated rate.

The regulatory landscape for gene therapy is constantly changing and global harmonization has yet to be aligned. An understanding of the regulations and guidance documents reflecting global regulatory agencies’ current thinking will help to better understand the key challenges. This is an exciting time in the industry with products being developed at an accelerated rate.

This webinar will discuss the current state of regulatory issues around gene therapy product development, key challenges for manufacturing controls and other insights in navigating the path to commercialization.

Register for this webinar to gain insights into:

  • Regulatory guidelines, with highlights from FDA’s gene therapy guidance documents issued in 2020
  • Challenges of following the traditional regulatory framework while trying to keep up with demand for cutting-edge treatments on accelerated timelines
  • Regulatory strategies with accelerated clinical plans — a comprehensive CMC plan and why early regulatory agency interactions will ensure long-term success
  • Establishing manufacturing controls and developing the appropriate analytical methods
  • Keeping up with gene therapy product development while identifying key challenges with high cost of goods, long lead times, manufacturing capacity, scale-up hurdles and increasing demands for plasmids (pDNA)
  • Future trends: how the global pandemic is shaping and/or repurposing emerging therapeutics

Join Dawn L. Wofford, Director, Regulatory Affairs, Cytovance Biologics in a live webinar on Thursday, March 4, 2021 at 12pm EST.

For more information, or to register for this event, visit Regulatory Strategies for Gene Therapy Product Development.

ABOUT XTALKS

Xtalks, powered by Honeycomb Worldwide Inc., is a leading provider of educational webinars to the global life science, food and medical device community. Every year, thousands of industry practitioners (from life science, food and medical device companies, private & academic research institutions, healthcare centers, etc.) turn to Xtalks for access to quality content. Xtalks helps Life Science professionals stay current with industry developments, trends and regulations. Xtalks webinars also provide perspectives on key issues from top industry thought leaders and service providers.

To learn more about Xtalks visit http://xtalks.com
For information about hosting a webinar visit http://xtalks.com/why-host-a-webinar/

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Sydney Perelmutter
Xtalks
+1 (416) 977-6555 x 352
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