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COVID-19 Diagnostics and Gene Therapy Regulation
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USITC report delves into patent rules' impact on COVID-19 diagnostics, with concerns about U.S. companies losing IP protections. The article also discusses the high costs of gene therapy for Sickle Cell Disease and the need for a regulatory process that enhances treatment options for immunocompromised individuals.
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How might the extension of compulsory licensing decisions on COVID-19 diagnostics impact the global pharmaceutical industry?
What are the potential implications of a regulatory process that enhances treatment options for immunocompromised individuals?
What strategies could be implemented to address the high costs of gene therapy for Sickle Cell Disease?
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