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Revolutionize Your Medical Device Product Development with Greenlight Guru

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.


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Revolutionizing Clinical Data Collection with Greenlight Guru

Empower Patients with Seamless Clinical Data Collection

Greenlight Guru's ePro Software enables the seamless collection of clinical outcome data through email/SMS, empowering patients to complete surveys anytime, anywhere, and on any device. Whether in-person, remotely, or through a combined approach, ePro Software revolutionizes how data is collected in the medical field.

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Enhancing Quality and Compliance with Greenlight Guru Audit Management Software

Streamlined Auditing Process for MedTech Companies

Greenlight Guru offers a comprehensive Audit Management Software that enables MedTech companies to seek out and eliminate inconsistencies and errors in their processes in an organized manner. This solution helps organizations keep up with their auditing schedules, assign tasks efficiently, and conduct audits with confidence. With over 1,100 of the world's leading MedTech companies trusting Greenlight Guru, this platform is designed to streamline and simplify the auditing process.

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Empower Your MedTech Teams with Greenlight Guru's Design Control Software

Streamlined Design Control Processes for Product Teams

Greenlight Guru's Design Control Software enables product teams in the MedTech industry to streamline their design processes, ensuring that no step is missed. With this solution, teams can focus more on product design and less on tedious paperwork. Additionally, the software facilitates collaboration among R&D teams for verification and validation testing. By linking all relevant documents, specifications, and design components with a single click, product teams can work efficiently and effectively.

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Accelerate Medical Device Development with Greenlight Guru Solutions

Streamlined Device Development Process

Greenlight Guru offers MedTech-specific solutions tailored to help companies accelerate their device development process. By seamlessly integrating design controls and risk management, businesses can ensure compliance and efficiency throughout their product lifecycle. This integrated approach eliminates manual processes, inadequate traceability, and the need for paper-based documentation, enabling teams to focus on innovation and speed to market.

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Enhancing Clinical Data Collection with Greenlight Guru’s Electronic Case Report Forms Software

Streamlined eCRF Solutions for MedTech Clinical Trials

Greenlight Guru offers a customizable eCRF software tailored to the specific needs of today’s MedTech industry. With this innovative solution, companies can design and implement effective eCRFs that enhance the quality and efficiency of clinical data collection.

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