Examines how pharma organizations must modernize information management to address regulatory complexity and global operations. Traditional siloed systems slow decision-making and increase compliance risks. Advocates for unified, cloud-based platforms that integrate structured and unstructured data. Emphasizes automation, AI, and analytics to streamline processes such as submissions, labeling, and compliance tracking. Highlights that efficient information management enables scalability, reduces errors, and creates a foundation for data-driven innovation in highly regulated environments.

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