How Painful Is Your Validation Process?

Simplifying 21 CFR Part 11 validation while improving audit readiness.

The validation process remains one of the most resource-intensive challenges facing life sciences organizations — especially as teams move faster, systems become more complex, and regulatory expectations continue to evolve.

Join Noverant for an interactive Lunch & Learn focused on practical approaches to automating validation for 21 CFR Part 11 regulated software applications. Designed for both growing biotech startups and established quality organizations, this session will explore how automated validation can reduce manual effort, improve consistency, and accelerate audit readiness without compromising compliance.

During this session, we will:

• Provide a concise refresher on 21 CFR Part 11 and current validation expectations
• Showcase an efficient, audit-ready validation package and supporting documentation
• Discuss practical strategies for reducing validation cycles and QA burden
• Open the floor for discussion, questions, and shared experiences from peers across the RTP biotech community

Whether your organization is building its first validated environment or modernizing mature quality systems, this session will offer practical insights into making validation faster, smarter, and more scalable.

Lunch will be provided.