Is Your QMS Stuck in the Past?

Nearly 50% of MedTech businesses are stuck with inefficiencies and outdated processes due to their paper-based or generic QMS.

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The Ugly Truth of a Paper-Based or Generic QMS

As technology rapidly changes how medical device companies operate, it’s clear that these outdated solutions simply don't work and hurt your bottom line.

Zero Traceability

Providing full transparency and visibility with a paper-based system is next to impossible. Documents will often get misplaced or stored in inaccessible locations. Multiple versions, missing signatures, and isolated processes lead to many failure points that ultimately affect your bottom line.

Lack of Efficiency

Generalized tools and systems require extensive customization to fit MedTech-specific regulations so you’ll face longer implementation times and constant validation concerns that can take months. Supporting older systems can also be non-intuitive, resulting in more training with a lack of support or slower response times.

Risk of Poor Quality

Poor quality management results in increased complaints, investigations, and CAPAs, tarnishing brand reputation and leading to higher product-related costs. A lack of real-time quality data also hinders informed decision-making, escalating the risk of adverse events that could have far-reaching impacts on patient safety and business viability.

It's Time to Upgrade to Greenlight Guru Quality

Specifically designed for MedTech companies, Greenlight Guru’s eQMS offers a modern solution to streamline design and development, connect your teams, and improve efficiency.

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The Benefits of Switching to a Modern QMS

Leave outdated methods behind, and embrace the modernization of a purpose-built eQMS to move your MedTech business forward. Streamline processes while minimizing costly errors so you can bring higher quality and safer devices to market faster.

Always Audit Ready

Your eQMS should be your source of truth. With Greenlight Guru, you'll have full visibility and traceability into any document, process, and procedure you need, so you can be prepared for any audit - even remote ones.

Compliance Made Easy

Greenlight Guru is designed to align with medical device regulations like ISO 13485 and FDA 21 CFR Part 820 without the need for extensive customization.

Improved Efficiency

Missing documents and signatures become a thing of the past. Greenlight Guru ties all your old processes into one streamlined platform. Key items are updated together through automated workflows eliminating multiple points of inefficiencies.

Built for Customers Like You

We're proud to work with over 1,100 of the best MedTech companies in the industry. Don't just take it from us. Discover what our customers have to say about us.

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Case Study

Puzzle Medical Beats Their Go-To-Market Timeline by 5 Months, Saving 360 Hours Per Employee/Year

"Greenlight Guru was instrumental in implementing our quality system. With them, we can bring safer, higher-quality medical devices to success while maintaining a quality culture ...

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Case Study

Monitored Therapeutics Inc. Passes 6 Audits and Scales Office by 7x Over 1 Year

“Purchasing Greenlight Guru was the best decision for our needs. Their easy-to-use eQMS, SOP Templates, and expert Guru guidance were key to us being able to successfully navigate ...

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Case Study