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Learn the most up to date recommendations and best practices from the ISO standard and how you can start to use risk management as a tool - not a checkbox activity.
The best QMS software comparison guide for medical device companies that will help you choose a quality management system solution that strategically benefits your product and company.
A free, in-depth webinar exploring what is and is not a regulated medical device and how manufacturers can interpret and leverage FDA's definition of a device.
A free, in-depth webinar covering the challenges medical device companies face today when demonstrating closed-loop traceability, the growing emphasis from industry standards and regulations, and the strategies, tactics, and tools device professionals can use to achieve truly connected quality.
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April 4, Coconut Berry Pops 0 Comments. Recent Posts. They bend over backw Having 20 years of medical device experience, I have worked with large and elaborate design controls and small and lean design controls.
I have also seen the disaster resulting from the absence of appropriate design controls. Greenlight Guru is exactly big enough to ensure compliance but small enough to be easily This is my first time going through a medical device product development process.
I've heard about all the challenges with Design Control. With Greenlight Guru, I know what to do and when to do it. Documenting Design Controls is really easy with this software.
When it comes to the way they have designed the fully integrated workflows exclusively for medical device and continue to innovate with new releases, I'd call them the Tesla of medical device eQMS software.
Greenlight Guru has made the design control and risk management process extremely easy to understand and explain to people not familiar with the process and helped them to understand how all of the steps are linked.
It has also made it significantly easier to get documentation reviewed and approved. Your software helped us tremendously in the last few months of , during which we had an important ISO audit.
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