PLM For Medical Devices Using Windchill
Air Date: July 21, 2016
If you’re actively looking for strategies to manage PLM for Medical Devices and comply with FDA standards, this TriStar webinar replay will be of value.
In this insightful session, you’ll discover how to:
- Effectively harness and manage essential data, including documents, BOMs, drawings, ECNs, and more, within the DHF, DMR, and DHR frameworks. These tools are vital for successfully navigating FDA audits, which many medical device manufacturers find challenging.
- Adopt a revolutionary method that goes beyond merely reporting data. Instead, you’ll learn to actively collect, manage, and monitor data through a dynamic dashboard that tracks progress throughout the product development cycle.
By the conclusion of this webinar replay, you’ll gain a clearer understanding of utilizing PTC’s Windchill to enhance your management of PLM for medical devices and ensure FDA compliance.
Manage PLM for Medical Devices to reach FDA Medical Device Compliance With PTC Windchill!
Thank you for joining the TriStar PLM Solutions webinar replay on PLM for Medical Devices and Device Compliance with the FDA using PTC Windchill. We hope you found the session both helpful and enlightening.
If you want to learn more about Windchill, we invite you to visit our Packages and Pricing Page. Delve into the details at your convenience to discover how our solutions can meet your needs.
Should you have any questions, our team is always ready and eager to assist you. Please don’t hesitate to contact us; we will reply quickly. Thank you for tuning in! Remember, partnering with TriStar means you gain full service and support, all tailored to enhance your business productivity!
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