Webinar Details
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Why You Should Attend
Medical device manufacturers are under more pressure than ever. Between escalating MDR/IVDR scrutiny, complex supply chains, and cost pressures, relying on paper travelers and manual processes is a significant business risk.
In this free, live webinar, you will learn how to:
- Achieve 100% UDI Traceability and execute flawless recalls in seconds, not days.
- Eliminate Paper DHRs and reduce DHR completion time by up to 80%.
- Enforce Process Validation in Perpetuity, providing auditors with continuous proof your process is in control.
- Shift from Detecting to Preventing quality issues with real-time SPC and closed-loop quality.
- Build a Tangible Business Case for MES with a proven ROI, including >30% reduction in cycle times and >15% reduction in scrap.
Who Should Attend
This webinar is designed for MedTech manufacturing leaders and professionals, including:
- VPs of Manufacturing & Directors of Operations
- Quality Managers & Directors (QA/RA)
- IT/OT Directors and Managers
- Process & Manufacturing Engineers
- Compliance and Regulatory Professionals
Meet Our Speakers
Chaitra brings deep expertise in implementing MES solutions that drive digital transformation and compliance in highly regulated environments.
With over 35 years in operational software and industrial controls at companies like Siemens and Rockwell, Maryanne focuses on partner strategy and go-to-market execution.
What You'll See: A Glimpse of the Live Demo
During the webinar, we will walk you through real-world scenarios in our MES platform:
- An Operator’s View: See a clean, intuitive interface for guided work instructions, component scanning, and digital work execution.
- A Quality Manager’s Dashboard: Witness real-time SPC charts, open non-conformances, and end-to-end lot genealogy in action.
Testimonials
Secure Your Place Today!
Don’t miss this opportunity to learn how to build a more traceable, efficient, and quality-driven manufacturing operation.