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FREE ON-DEMAND WEBINAR

3 Ways to Transform your Change Process through AI-powered Predictive Quality

Change management can be a daunting task for medical device companies.

Most quality solutions make the process of identifying every document impacted by a proposed change order tedious and error-prone, requiring either encyclopedic knowledge of a company's QMS or labor-intensive searches through endless files.

Our 2021 State of Medical Device Benchmark Report uncovered that 60% of medical device professionals say they rely on traceability for conducting changes with 28% reporting it takes a full day to run a change impact analysis.

These findings reveal two mission critical factors associated with conducting a change: traceability and time.

The unfortunate truth for many companies is that these resources are limited or nonexistent, leaving teams with no other option but to manage change through a reactive process that's fraught with mistakes, rework, and unpredictability.

This free, in-depth webinar, presented by industry leaders in medical device quality at Greenlight Guru, will show you how to transform your change management process through predictive quality, which leverages AI/ML technologies to enable and promote proactive decision-making and full visibility throughout the change process.

FREE PRODUCT BONUS: All registrants will get an exclusive look into the software functionality of Greenlight Guru's latest release, Halo℠ for Change Management — the world’s first AI/ML recommendation engine for medical device quality that revolutionizes the change management process.

Watch the webinar

GG webinar - 2-11-21
Specifically, this webinar will cover:
  • Current industry challenges around reactive change management practices
  • Capabilities of AI and machine learning (ML) technologies within a medical device quality system
  • Proven strategies for advancing your current change management process
  • How to switch from reactive to predictive quality management so you can understand the downstream impact of a change and reduce the number of missed documents
  • Q&A session
Who Should Attend?
  • Quality Professionals and Management
  • R&D Engineers and Management
  • Medical Device Executives
  • Regulatory Affairs Professionals and Management
  • Clinical Affairs Professionals and Management
Register Now

Hosted by

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Presenter: Tom Rish

Manager, Medical Device Gurus, Greenlight Guru

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Moderator: Jon Speer

Founder, Greenlight Guru

loopMark

About Greenlight Guru

Greenlight Guru is the only quality management software platform designed specifically for medical device companies. The platform helps companies bring safer products to market faster, simplifies FDA and ISO regulatory compliance and provides a single source of truth by connecting the management of all quality processes like CAPAs, risk, audits and more. Greenlight Guru’s platform is used by thousands of users across the globe to push beyond baseline compliance and achieve True Quality for their medical devices.

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