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Guiding Science and Law of Generic Drug Equivalence Testing
Generic drugs are often seen as a cost-effective alternative to their brand-name counterparts and have the potential to save consumers billions of dollars. But how can we be sure that generic drugs are equivalent in quality and efficacy to their brand-name counterparts? In this blog post, we will explore the science and law behind generic drug equivalence testing and take an inspiring look into the future of generic equivalent drugs. We will discuss the science behind generic drug equivalence testing, US law and regulations surrounding the process, and new developments in this field. By the end of this post, you will have a better understanding of how generic drug equivalence…
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Legal Landscape of Generic Drug Development for Future Innovation
The legal landscape of generic drug development is complex and ever-evolving. As new treatments and medicines are developed, changes in the law must be made to support the innovation process. In this blog post, we will examine the legal requirements for generic drug development and the implications of these laws for future innovation. We will also discuss any exemptions to the law and how they may affect innovation. By the end of this post, you should have a good understanding of the legal landscape of generic drug development and its implications for future innovation. Read More: Marcy Resnik What are the Legal Requirements for Generic Drug Development? Generic drug development…