You're expected to maintain compliance while increasing throughput, reducing review times, and driving continuous improvement. But your tools weren’t designed for that.
In this upcoming webinar, learn how leading medical device manufacturers are moving beyond documentation-driven processes to build operations that are agile, traceable, and built for continuous improvement. See how teams are capturing genealogy data in context, surfacing nonconformances in real time, and simplifying final reviews with connected, configurable workflows.We’ll explore how to go beyond digitalization and create a system where compliance supports innovation, powered by a composable platform built for validation, speed, and traceability.
What You'll Learn:
Maintaining Compliance—and Progressing Innovations: Why static systems limit traceability, delay reviews, and block improvement; and how modular tools are changing the game.
Live Demo: Build a Smarter Workflow in Minutes: Watch us assemble a production workflow that captures genealogy data, flags nonconformances, and supports validation — no IT team needed.
Turn Disruption Into an Advantage: See how real-time alerts and connected systems help teams act fast, fix faster, and keep operations audit-ready at every step.
What Leading Med Device Teams Are Doing Differently: Hear how manufacturers like Outset Medical are moving faster, with fewer errors, and without compromising compliance.
If your team is looking to modernize quality, simplify traceability, and adapt faster without revalidating entire systems, this session will show you what’s possible.
Featuring:
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Michelle Vuolo
Head of Quality | Tulip
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Jeff Ashton
Digital Transformation Engineer | Tulip