UPCOMING WEBINAR

The Right-First-Time Factory: Building a Culture of Proactive Quality in Pharma

Thursday, September 4th - 11 AM ET / 10 AM CT

In pharma, the margin for error is zero. You’re expected to uphold the highest GMP standards, protect data integrity, and hit right‑first‑time production — every time. But manual batch records, reactive quality systems, and delays in deviation management make that mission harder with every new product and every new market.

In this upcoming webinar, you’ll learn how top CDMOs and pharma manufacturers are building a culture of proactive quality, not just compliance. See how digital workflows guide operators, enforce ALCOA+ at the point of execution, and shrink deviation risk before it starts.

We’ll show you how to create an operation that audits itself, adapts in real time, and gets closer to instant batch release with every run.

What You’ll Learn:

  • Why Quality Needs to Be Proactive, Not Reactive: How traditional systems introduce risk, delay batch release, and slow down innovation—and how a new model helps fix that.

  • Live Demo: Continuous Transformation in Action: Watch us build, deploy, and refine a quality inspection app on the spot — demonstrating how composability enables rapid iteration and frontline-led change.

  • Digital Workflows that Enforce GMP in Real Time: See how guided execution, automatic data capture, and real‑time checks create an environment of audit-ready, right‑first‑time production.

  • How Leading Pharma Teams Are Reducing Batch Release Time: Learn how CDMOs are cutting review cycles and driving continuous improvement without compromising compliance.

If you’re under pressure to reduce deviation rates, accelerate tech transfer, and improve batch performance, this session will show you where to start.

Featuring:

  • Headshot of Michelle Vuolo

    Michelle Vuolo

    Head of Quality | Tulip

  • headshot

    Jeff Ashton

    Digital Transformation Engineer | Tulip