The race to bring innovative therapies to market is more competitive and urgent than ever. Artificial intelligence (AI)-powered automation within life sciences regulatory information management (RIM) offers a transformative solution for accelerating time to market. The future of RIM is no longer a distant vision. It is a present reality driven by the urgent need for efficiency, accuracy, and compliance in an increasingly complex regulatory environment.
Join us for an executive-level webinar with speakers Bill Engle, Vice President and AI-powered automation lead at CGI, Joe Miles, Industry Director for Life Sciences at UiPath, and Nicole Falk, Director and Life Sciences consulting lead at CGI, to explore how AI and automation are becoming a strategic imperative for maintaining competitive edge and regulatory compliance in 2024 and beyond.
Key topics include:
- AI-powered RIM: Transforming regulatory workflows and decision-making processes
- Quick-value use cases: Streamlining submission preparation and regulatory correspondence
- ROI of AI and automation: Cost savings, efficiency gains, and error reduction in RIM
Don’t miss this opportunity to gain insights into the future of RIM and how AI-powered automation can give your organization a competitive advantage in navigating the complex regulatory landscape. Register today.
Key Objectives:
- Opportunities to transform regulatory workflows and decision-making with AI-powered automation.
- Familiarity with use cases to kickstart adoption of AI-powered automation with quick wins.
- Understanding the return on investment of automation of RIM processes for life sciences.