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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.
Manufacturing, Quality, and Asset Management — Simplified with Life Sciences-Specialized AI.
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.
Manufacturing, Quality, and Asset Management — Simplified with Life Sciences-Specialized AI.
As a Sr. Product Marketing Manager at MasterControl, Nicole Sherman is focused on data analytics and artificial intelligence. She focuses on understanding the current market landscape and partnering with other departments to help communicate valuable product benefits that meet market needs. This includes go-to market strategy, product positioning messaging, launch communications, and more.