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Greenlight Guru

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510 reviews
  • 4 profiles
  • 4 categories
Average star rating
4.5
#1 in 1 categories
Grid® leader
Serving customers since
2013
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Greenlight Guru Quality Management System

401 reviews

Greenlight Guru is the only quality management platform designed specifically for medical device companies.

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Greenlight Guru Clinical

109 reviews

State-of-the-art data collection, storage and productivity tool for organisations that need to generate and manage clinical evidence.

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Enzyme QMS

0 reviews

Enzyme QMS is designed for medical device, digital health, and biopharma companies.

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Enzyme

0 reviews

Enzyme is an all-in-one platform designed to simplify the process of launching and managing web3 projects by enabling users to discover, deploy, and oversee smart contracts without requiring technical expertise. By offering a user-friendly interface and a comprehensive suite of tools, Enzyme empowers brands, creators, agencies, and developers to seamlessly integrate blockchain technology into their initiatives. Key Features and Functionality: - Discover: Access a vast library of pre-built and securely audited smart contracts across various categories, ready for immediate deployment. - Deploy: Launch smart contracts on supported blockchains, including Ethereum and Polygon, without any prior blockchain experience. - Manage: Utilize intuitive dashboards to oversee all aspects of your smart contracts, including those imported from external sources, with options for both public and private views. - Customizable Sales Pages: Create and publish no-code, customizable sales pages for digital collectibles, or embed minting buttons directly into your website within seconds. - Zero Transaction Fees: Deploy publicly available smart contracts without incurring transaction fees, apart from standard deployment gas fees. - Security: Built on top of battle-tested libraries of smart contracts by OpenZeppelin, ensuring robust and secure operations. Primary Value and User Solutions: Enzyme addresses the complexities and technical barriers associated with entering the web3 space by providing a streamlined, no-code solution for deploying and managing smart contracts. This accessibility allows users without technical backgrounds to leverage blockchain technology effectively, facilitating the creation of decentralized applications, NFT collections, and other web3 projects. By eliminating the need for extensive coding knowledge and offering a suite of supportive tools, Enzyme accelerates the development process and broadens participation in the blockchain ecosystem.

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361
125
17
4
3

Greenlight Guru Reviews

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Profile Name
Star Rating
361
125
17
4
3
Verified User in Medical Devices
UM
Verified User in Medical Devices
11/28/2025
Validated Reviewer
Verified Current User
Review source: Organic

GreenLight Guru QMS

Addition of features such as supplier grouping have made the system more functional.
Leslimar P.
LP
Leslimar P.
11/24/2025
Validated Reviewer
Verified Current User
Review source: Organic

All-in-One Training Tools That Exceed Expectations

Excellent server that offers the necessary training tools in one place.
Verified User in Medical Devices
AM
Verified User in Medical Devices
10/29/2025
Validated Reviewer
Verified Current User
Review source: Organic

Best QMS for Medical Device Design Firms—Robust Features, Stellar Support, Minor Analytics Gaps

GG is the best eQMS for traditional medical device design and development (can't speak for software dev). We looked at many systems but would have had to keep our design matrices and risk in excel. The design workspace is build to ISO 13485 and allows you to link your design items to relevant documents and related risk items. You can document design reviews in software and print a simple design file. Risk is built to ISO 14971 and doesn't trap you into just FMEA. It incorporates harmonized IMDRF terms for hazards and harms and includes various regulatory codes, which is great for regulatory reporting. You can review and lock your risk analysis in a way that makes it easy for risk to stay a living "document". You can view documents in app, which is surprisingly not a feature for many systems and a must have for me. Attributes and tags make it easy to organize and find documents. Change management is flexible and allows you to route multiple documents at a time. Training is great, I can automate SOP training so nothing gets missed. The quality events could be improved but are workable and you can link audits to CAPAs to risk to documents which is great. Admin has got to be the easiest of any out of the box software and the support is world class. If you want a super custom system, this probably isn't for you. If you need a quick and straightforward implementation and are happy with a system built for ISO 13485 and ISO 14971 take a look! We were mostly implemented in 3 months and fully implemented by 5 with everyone trained! Almost all of the users find it intuitive to join, train, and sign off on change and documents. Users that use it for quality events, design, risk, and admin were able to feel comfortable very quickly.

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HQ Location:
Indianapolis, IN

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@greenlightguru

What is Greenlight Guru?

Greenlight Guru is a leading quality management software platform designed specifically for medical device companies. It offers tools that streamline the product development process, ensure compliance with regulatory standards, and facilitate collaboration among teams. By providing comprehensive solutions for document management, risk management, and training, Greenlight Guru helps organizations enhance their quality processes and accelerate time-to-market for medical devices. For more information, visit their website at https://www.greenlight.guru/.

Details

Year Founded
2013