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Managing Postmarket Quality

Risk Less & Succeed More with Postmarket Quality

22% of companies that were issued a warning letter take over 3 years to fully resolve them. Invest in a purpose-built solution and avoid that risk. Establish robust postmarket quality processes with a powerful QMS so your team is ready when a complaint surfaces or an auditor comes knocking.

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Start Early

The biggest mistake a company can make during the transition to postmarket is not having quality processes streamlined in advance. You need to have confidence in your CAPA, Audit, Nonconformance, and Complaint handling processes now. If you don’t, the consequences can be costly. Choose a QMS that supports your development and quality processes throughout your entire product lifecycle.

800+ of the world’s leading MedTech companies trust Greenlight Guru.

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Quality Workspaces That Support Your Product Lifecycle

Keep your products on the market and ensure safety for your patients.

Streamline Processes

Your quality workspaces should have a framework to guide you. Whether it’s a CAPA or complaint, you and your team need to collaborate and strategize next steps.

Collaborate Effectively

Our quality workspaces enable you to work better with your peers. Assign tasks, link documents or design artifacts, create action items, investigate root cause, and generate critical documentation.

Enhance Visibility

Your connected Greenlight Guru ecosystem gives your team visibility into the investigation.

Continuous Improvement

Learn from the catalyst that caused the quality event to take place. Make your devices better and stronger with each update.

How Greenlight Guru Can Help

Uncover all of the ways our end-to-end solution built specifically for the MedTech industry can get you on the right track to prepare for regulatory submissions.

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Are You Ready to Experience the Greenlight Guru Difference?

With solutions to improve every stage of your product lifecycle and a team excited to support you, achieving excellence has never been easier.

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