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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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Nonconformance Management Software

A Simplified Way
To Manage Nonconformances

Once identified, a nonconformance can and should be handled efficiently. Uncover, investigate, and address them as they happen so your teams can quickly get back to innovating.

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1,000+ of the world’s leading MedTech companies trust Greenlight Guru.

Nonconformance-1

Don’t Let a Nonconformance
Set You Back

Investigating a nonconformance can be an intensive process, involving careful scrutiny of details and paperwork. Creating action items, effectively documenting them, and then generating an appropriate response can feel like an impossible task. It's easy to get lost, especially when the next steps aren't clear. Greenlight Guru provides a solution that brings all of your necessary documents and procedures together in one place.
loopMark

A Straightforward Approach to Nonconformances

Leverage Greenlight Guru’s Nonconformance Management Software to guide you through the essential processes while giving you the flexibility you require to link anything anywhere.

Connected Ecosystem

Access tasks, sources, QMS documentation, and next steps—all in one place.
Establish Workflows

Greenlight Guru provides you with a defined workflow so you can address the nonconformance and determine the root cause.
Gain Efficiency

Automate your workflow inside your QMS to help you track the correct action items to the right user or group.
Solve Problems

Improve the quality of your medical devices and get ahead of time-consuming and expensive issues.

Efficiently Address and Take Actions on Nonconformances

Designed specifically for the MedTech industry with flexibility in mind.

A Defined Path To Address Nonconformance

See each stage required to close out a nonconformance.

Streamline Team Management and Scheduling Deadlines

Assess, plan, and schedule your nonconformance in detail.

An Easy Review Process

Have your nonconformance team review the work and provide e-signatures for approvals.
Designed With Your Entire Organization in Mind

Benefits for Teams

Not addressing a nonconformance right the first time can lead to even more expensive and time-consuming delays down the road.

For Product Teams

Ensure your devices continue to grow and excel

  • Keep up with your devices as they change
  • Take a critical part in determining next steps and performing investigative tasks
  • Provide insights and solutions
Designed With Your Entire Organization in Mind

Benefits for Teams

Not addressing a nonconformance right the first time can lead to even more expensive and time-consuming delays down the road.

For Quality Teams

Go after nonconformances with confidence

  • Stay compliant throughout the process
  • Share findings with other teams so the necessary actions and changes are implemented
  • Advocate for the quality of your devices

For Executive Teams

Ensure the continuous success of your product lines

  • Keep teams efficient with an all-in-one solution
  • Ensure safe product lines
  • Enable your teams to collaborate

See More of Our Nonconformance Workspace

Check out our straightforward and thorough ways to handle nonconformances for your medical devices.

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$ 125 k

saved on average per project

3

months faster to market

402

hours saved on low value-added activities
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