Modernizing Data Governance and Workflow Automation for Life Sciences Innovation

In the fast-paced world of biotech and pharma, the pressure to accelerate drug development is immense. However, this race for innovation is often hindered by a silent, but significant, challenge: unmanaged data. From clinical trials to in-licensing agreements, data sprawl and manual processes can create compliance risks, impede collaboration, and slow down time to market.

Join our panel of experts to explore how modernizing your data governance strategy is not just about meeting regulatory requirements like GxP and 21 CFR Part 11, but about unlocking innovation. This session will dive into the data dilemmas faced by the modern biotechs and demonstrate how a Modern Content Management platform, combined with intelligent workflow automation, enables secure, compliant, and efficient data flows.

We will discuss how a single, centralized platform can:

• Navigate the data deluge: Bring order to the massive amounts of data generated from genomic sequencing, research, and clinical trials.

• Ensure regulatory readiness: Maintain audit trails and granular access controls for sensitive data, ensuring adherence to strict guidelines like ALCOA+.

• Streamline complex processes: See a real-world example of how a digital biotech used Egnyte to simplify the in-licensing of thousands of clinical records.

• Democratize data for more intelligent insights: Learn how metadata-driven data flows can make research and clinical data more accessible and usable.

This webinar is for any life sciences professionals in IT, Business Operations, and Compliance who want to transform their data challenges into a competitive advantage.