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In today's complex regulatory landscape, life sciences professionals spend countless hours firefighting document management challenges rather than focusing on strategic quality initiatives. From missing signatures and lack of competency to translation errors and failed audits, document management inefficiencies consistently rank among top reasons for FDA citations and quality defects globally.
This webinar explores how intelligent document management is revolutionizing quality processes across pharmaceutical, biotech, and medical device companies. Through real-world scenarios and a "day in the life" perspective, we'll demonstrate how document errors create costly downstream consequences that impact regulatory compliance, operational efficiency, and ultimately patient safety.
Learn how innovative technologies—including advanced data analytics, AI-powered translation and summarization, automated workflows, regulatory intelligence, and more—are transforming traditionally manual, error-prone processes into strategic assets that enhance compliance and operational excellence.
Jessica is the Sr. Product Marketing Manager over MasterControl Quality Excellence. She has an extensive marketing career spanning nearly 20 years including leadership, strategy, product marketing, customer marketing, and demand gen. Jessica excels at working across teams to bring products to market and translating tech features to customer benefits that resonate.