Greenlight Guru's MD QMS software is designed specifically to fit the needs of the medical device industry. Companies that must comply with industry regulations, like ISO 13485, 21 CFR Part 820, EU MDR, etc,, use Greenlight Guru's MD QMS to streamline their product development and quality processes to ensure compliance as it provides. From product development, quality and regulatory, to partners and company executives, everyone on your team can benefit from using Greenlight Guru.
Greenlight Guru's eQMS software benefits product development, quality, and executive teams by:
- Streamlining the management of device requirements, risk, design reviews, and documentation.
- Driving traceability throughout your quality, design, and risk processes.
- Assure your team's documentation is audit ready in real time.
- Enhancing collaboration efforts between teams to accelerate development and improve the quality of regulatory submissions
- Leveraging quality as a strategic advantage to protect your brand and impact the top and bottom lines
Greenlight Guru is an out-of-the-box solution that is easy to use and intuitive for users of all technical backgrounds. Their purpose-built solution alleviates all of the time consuming effort that would go into the implementation, configuration, and validation of a general purpose solution making it nearly effortless for customers to use. Because their quality management software is 100% cloud-based, all users can access Greenlight Guru via a standard web browser enabling better collaboration and efficiency throughout a companies product’s lifecycle.
As the only quality management system purpose-built for the needs of medical device companies, Greenlight Guru is leading companies in more than 600 cities in 50 countries on 6 continents implement their quality culture using their software. With over 75 years of industry experience on their team, Greenlight Guru has produced the industry's #1 blog, podcast, and webinar that over 68,000 people rely on for the latest news in quality for medical devices. Why not choose the industry leading software designed by industry leaders?
Greenlight Guru is commonly assessed next to competitors like paper-based quality systems, general purpose office tools, and general purpose legacy softwares, like MasterControl and Arena.
Greenlight Guru is an out-of-the-box solution that is easy to use and requires no additional configuration that could prolong implementation and/or validation efforts. Their MD QMS software automates quality processes, helps teams achieve end-to-end traceability, and streamlines team collaboration with built-in controls to follow FDA and ISO best practices.
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Pre-market Quality Management Software - helps you set a quality foundation to bring safer, high-quality medical devices to market faster.
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Post-market Quality Management Software - provides visibility into post market activities to decrease risk so you can advance the success of your medical device(s).
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Quality Management Experts - help you establish and advance a quality culture throughout your company and the entire lifecycle of your device.
Every customer is paired with a dedicated medical device industry expert to schedule live sessions to guide you through the on-boarding process and get your team up to speed with using Greenlight Guru's software. The in-app Help Center also allows customers to access training and support articles and videos on navigating the software.
For customers that need supplemental on-boarding or training services, the team at Greenlight Guru will work with you to define an extended scope of training and advising for software best practices and next steps to guide your team to specific milestones in your quality transformation. They are also capable of consulting and guiding you through product development activities, preparation for regulatory submissions, gaining certification, and much more.
Depending on the prioritized use case for your company, this transition time to value can be seen within two to eight weeks. The team at Greenlight Guru will work with you to define and establish a plan for transitioning existing documentation and a dedicated medical device industry expert will work closely with you to define how your processes will translate into your eQMS with Greenlight Guru.
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