Streamlined Development Processes
Greenlight Guru offers a comprehensive solution to automate tasks that typically delay medical device development. By simplifying design control matrices, change orders, design reviews, and DHF management, Greenlight Guru enables companies to transition hours of work into a few simple clicks. This streamlines the development process, allowing organizations to bring their products to market faster and more efficiently.
Customer Benefits
Clients using Greenlight Guru experience significant improvements in various aspects of their development process. On average, customers report a 35% reduction in time to market, a 50% decrease in time spent on development and design documentation, and a 35% reduction in manual hours required per recall or adverse event. Notably, Greenlight Guru has saved its users an average of 144 hours with automated Design History File (DHF) management. Testimonials from satisfied clients, such as Nick Punsalan from MicroAire Surgical Instruments, highlight the exceptional time savings Greenlight Guru provides.
Comprehensive Solutions
Greenlight Guru's product development software covers a wide range of functionalities essential for medical device companies. From document management to risk management, change control, training management, CAPA, complaint management, nonconformance handling, project management, audit management, supplier management, and more, Greenlight Guru offers a comprehensive suite of tools to support every stage of the product development lifecycle.
Resourceful Support and Resources
Greenlight Guru not only provides innovative software solutions but also offers a wealth of support and resources to its users. The platform includes a ROI calculator to quantify the benefits of using the software, a blog with the latest news and industry insights, a medical device glossary, podcasts, webinars, events, customer stories, checklists, templates, eBooks, guides, and thought leadership articles. Additionally, Greenlight Guru has been featured in the G2 Crowd Report and offers valuable comparisons with competitors like MasterControl, Arena Solutions, and Qualio.
Regulatory Compliance and Best Practices
In the highly regulated medical device industry, compliance with quality standards and regulations is crucial. Greenlight Guru supports companies in achieving and maintaining compliance with standards such as ISO 13485, ISO 14971, ISO 14155:2020, 21 CFR Part 820, and 21 CFR Part 11. By offering insights into design controls, CAPA, IQ, OQ, PQ, EDC Systems, and eCRF, Greenlight Guru empowers organizations to meet regulatory requirements and industry best practices.