Author Archives: Santosh Shevade

Part 2: How Generative AI is Transforming Regulatory Submissions in Pharma R&D

Part 2: How Generative AI is Transforming Regulatory Submissions in Pharma R&D

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In Part 2, we explore how Generative AI can revolutionize regulatory submissions in pharmaceutical R&D, addressing data management, compliance, and collaboration challenges while acknowledging the transformation’s inherent complexities and obstacles.
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Part 1: How to Decode Regulatory Submissions in Pharma R&D?

Part 1: How to Decode Regulatory Submissions in Pharma R&D?

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Each region, including the U.S. (FDA), the European Union (EMA), and others, has specific submission requirements, making the process more complex due to varying content and structure guidelines across jurisdictions. Read More

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