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More than a Quality Management System: Tools for the entire MedTech Lifecycle.

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Featured Capabilities:

Document Management Training Management Product Development Design Control Risk Management CAPA Management Audit Management

Experience the #1 QMS software for medical device companies first-hand. Click through an interactive demo.

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Data collection and management designed for MedTech clinical trials.

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Featured Capabilities:

Electronic Data Capture (EDC) Electronic Case Report Forms (eCRF) Electronic Patient Reported Outcomes (ePRO) Ad-Hoc Data Collection (Cases) Post-Market Surveys Product Add-Ons

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Ultimate Guide to Comparing Quality Management System Solutions

This eBook compares the best QMS software solutions to help medical device companies make an informed decision when investing in a quality management system.

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FREE LIVE DEMO
February 8, 2024

Integrating Risk Management Throughout the Entire Device Lifecycle with Greenlight Guru Quality

Join us for an exclusive live demonstration of Greenlight Guru's latest Risk Management Software, tailored for medical devices.

This demo is a unique opportunity to see how our software aligns with ISO 14971:2019, ensuring compliance and fostering collaboration for enhanced product safety, accelerated time-to-market, and streamlined post-market activities.

In this 30-minute session, you'll experience:

  • Integrated Risk Management: Uncover methods to weave risk-based thinking throughout your device ecosystem, ensuring adherence to both ISO 14971:2019 and ISO 13485:2016 standards.
  • Intuitive Risk Matrix: Explore our user-friendly interface to proactively identify and mitigate potential risks early in the development process.
  • Seamless Connection to Design: Discover the simplicity of integrating risk control measures with design controls and documents, effectively minimizing lifecycle risks.
  • Robust Risk Management File Creation: Learn how to use our software to assemble a thorough, audit-ready Risk Management File effortlessly.
  • End-to-End Traceability: Witness the benefits of a cohesive risk management strategy that spans from initial design to post-market analysis, ensuring full lifecycle traceability.

Register now to secure your spot!

Watch now
GG Quality Live Demo 2-8-24
Who should attend?
This demo is essential for MedTech risk managers and product development professionals seeking to enhance their risk management strategies with cutting-edge solutions.
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Hosted by

Laura Court
Laura Court

Solutions Engineer,
Greenlight Guru Quality

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About Greenlight Guru

Greenlight Guru is the #1 provider of modern cloud-based solutions for the MedTech industry, helping companies bring life-changing products to market faster, more efficiently, and with less risk.

Greenlight Guru’s MedTech Suite provides quality management, product development, and clinical data management solutions, along with high-quality training and education required to keep up with the rapidly changing industry regulations.

Trusted by over 1,100 medical device companies across the globe, Greenlight Guru has been named by G2 as the #1 Medical QMS Software and by the Inc Magazine as a Best Place to Work.

Visit our homepage to learn more.

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