How Painful Is Your Validation Process?

Overview

Join Noverant on August 5 for an interactive lunch and 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.

This session will:

Provide a concise refresher on 21 CFR Part 11 and current validation expectations
Showcase an efficient, audit-ready validation package and supporting documentation
Offer 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.

August 5, 2026 11:00am - August 5, 2026 12:00pm

NCBiotech
15 TW Alexander Dr.
Durham, NC 27713

No Cost

Biomanufacturing

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