Skip to content

UPCOMING WEBINAR

Tulip in Action: Digitizing eDHRs for Medical Device

Thursday, October 23rd | 1 PM ET

A Hands-On Demo of Tulip for Regulated Manufacturing

Curious how Tulip supports compliance, quality, and agility in real-world medical device operations? This hands-on session walks you through a complete demo of the platform in action — showing how manufacturers digitize Device History Records (eDHRs), error-proof workflows, and streamline review cycles.

We’ll walk through a live nebulizer assembly use case from start to finish: selecting a prebuilt app, customizing it for compliance needs, and deploying it in a virtual environment. You’ll see how fast and easy it is to go from idea to impact — with no code and no IT delays.

You’ll see how to:

  • Launch and adapt an eDHR app from Tulip’s Library
  • Customize forms and logic to guide operators through regulated workflows
  • Connect machines and test equipment for automatic data capture
  • Ensure traceability and compliance across the full assembly process

Register now and see how leading MD&D teams are replacing paper, reducing errors, and staying audit-ready — without slowing down.

Featuring:

  • A headshot of a tulip employee - Sean Joseph

    Sean Joseph

    Engineer, Tulip