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The Covid-19 pandemic highlighted the importance of the healthcare market being able to bring new and improved treatments to patients faster. From regulators and pharmacovigilance teams to clinical developers and academic researchers and many others in between, the healthcare ecosystem demonstrated how effectively it can operate in a very short space of time. As innovations are developed in laboratories, and throughout the drug development lifecycle, regulatory is at the center of project teams helping to ensure treatments get approval as expeditiously as possible.
Download now to explore this challenge in detail, explaining the difficulties faced by regulatory affairs leaders and how regulatory intelligence solutions powered by artificial intelligence offer a path to enhancing efficiency and accelerating approvals. Further, it will introduce solutions designed to instigate a simple and quick way of querying critical documents to understand past approvals and related communications from health authorities.
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