Greenlight Guru has also maintained a Leader position in the Medical QMS software category for five consecutive quarters with an overall satisfaction score of 97 - three points greater than the nearest competing product. As the only QMS exclusively built for medical device success, Greenlight Guru is proud to be trusted by leading, life-saving medical device companies globally.
Learn more about our Spring Report Scores on our blog!
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An efficient and controlled way of managing our documentation is now much more straightforward. I am confident that we are compliant with using GG
Greenlight Guru are ahead of the game in terms of incorporating workflows which lead to compliance to ISO 13485:2016 and 21 CFR Part 820 regulations. The Change Management and Document Control functionalities make it easy to control records and document approvals especially in a world that is moving away from the traditional 'in-office' setting to remote working
The software is user-friendly and customizable enough to meet your needs if you already have an existing QMS set up. But honestly, the best part is the team we work with for our transition process. They make the difference in this being a good experience. Their friendliness and wealth of knowledge about the medical device industry made the process so easy
With Greenlight Guru, we have been able to solve training gaps, on-time completion of customer complaints and non-conformances, and change orders. Previously to Greenlight, we had complaints that sat uncompleted for over a year; now with GG we are able to close them in less than 30 days.
Greenlight Guru is life-changing! The platforms for documentation and collaboration have made me and my team so much more efficient. It has turned the huge headache of regulatory compliance into a much more manageable task.
Fantastic support, complete documentation package which just needs minor adjustments to suit the company, intuitive navigation through the menu, and different QMS modules inside the software.