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Molecular Med TriCon 2019 | Gene Therapy for Rare Disorders
Manage episode 248298673 series 31038
Content provided by CHI Podcasts and Cambridge Healthtech Podcasts. All podcast content including episodes, graphics, and podcast descriptions are uploaded and provided directly by CHI Podcasts and Cambridge Healthtech Podcasts or their podcast platform partner. If you believe someone is using your copyrighted work without your permission, you can follow the process outlined here https://ro.player.fm/legal.
Gene therapy presents a promising path ahead for patients of rare diseases. The United States Food and Drug Administration’s Director of the Center for Biologics Evaluation and Research, Dr. Peter Marks discusses his work advancing production and availability of gene therapies for rare disorders, and the unique challenges to producing efficacious therapeutics in this field. For more information, please visit https://www.TriConference.com/Gene-Therapy
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255 episoade
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Manage episode 248298673 series 31038
Content provided by CHI Podcasts and Cambridge Healthtech Podcasts. All podcast content including episodes, graphics, and podcast descriptions are uploaded and provided directly by CHI Podcasts and Cambridge Healthtech Podcasts or their podcast platform partner. If you believe someone is using your copyrighted work without your permission, you can follow the process outlined here https://ro.player.fm/legal.
Gene therapy presents a promising path ahead for patients of rare diseases. The United States Food and Drug Administration’s Director of the Center for Biologics Evaluation and Research, Dr. Peter Marks discusses his work advancing production and availability of gene therapies for rare disorders, and the unique challenges to producing efficacious therapeutics in this field. For more information, please visit https://www.TriConference.com/Gene-Therapy
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255 episoade
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