QMS COMPARISON

Greenlight Guru vs Arena Solutions?

Arena Solutions offers product lifecycle management (PLM) and QMS solutions for various industries with a product-centric focus, while Greenlight Guru provides a MedTech-specific eQMS ensuring compliance without the need for complex customizations.

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What's the Difference?

Arena specializes in PLM software that helps manufacturers across multiple industries facilitate the flow of product-related information through development.

Greenlight Guru’s QMS software is designed specifically for the unique needs of MedTech. It empowers teams looking to enhance speed and quality while lowering risk and costs.

While Arena offers a QMS, it is not industry-specific. It needs extensive customizations to meet the compliance standards for MedTech. Greenlight Guru's fully validated solution helps you get to market faster and stay in market longer.

Learn More about PLM vs QMS

QMS Comparison

We understand that you're not just buying software, you're investing in an outcome for your medical device business. You'll need an eQMS built for your objectives.

Purpose-built for medical device companies

Ranked #1 eQMS for medical device companies

Offers both eQMS and EDC solutions

Risk management functionality compliant with ISO 14971

Ranked "Best Support" and "Fastest Implementation" on G2

Library of over 70 Audit-Tested SOP templates

Modern user interface

Team of experienced Industry Gurus

Supports Pre-Market and Post-Market Activities

Purpose-built for medical device companies

Ranked #1 eQMS for medical device companies

Offers both eQMS and EDC solutions

Risk management functionality compliant with ISO 14971

Ranked "Best Support" and "Fastest Implementation" on G2

Library of over 70 Audit-Tested SOP templates

Modern user interface

Team of experienced Industry Gurus

Supports Pre-Market and Post-Market Activities

Top Reasons Companies Choose Greenlight Guru

Greenlight Guru empowers companies to move faster, become more efficient and minimize risk.

Efficiency in Design and Risk Management

Greenlight Guru’s design and risk management tools streamline development processes and traceability, so you can innovate faster while ensuring compliance.

Ease of Use and Interface

Greenlight Guru's intuitive interface and flexible document management system enhance the user experience, making it easier to manage quality processes seamlessly.

Customer Support

Our dedicated success managers help you navigate each stage of your medical device journey with industry-specific expertise so you can meet your goals faster.

Compliance and Validation

Our purpose-built solution aligns with FDA standards and international standards, including ISO 14971 and ISO 13485, and simplifies the validation documentation processes without extra costs.

Customer Satisfaction Ratings

See how real customers rated Greenlight Guru and Arena Solutions’ abilities to satisfy their needs.

Source from G2 Winter 24 Report

What G2 Users Have to Say

“Implementing the design controls and risk management activities is intuitive. It is making life easy to trace and immediately generate the necessary reports.”

Sravan Kumar M.

Medical Device Quality & Regulatory Consultant

“In my opinion, the best features are the ability to link anything (documents, training, Audits, CAPA, NCs) to one another. flexible document management with customisable values and attributes, and the overall UI.”

Anna A.

Greenlight Guru Customer

“The customer support team at Greenlight is incredible, and we've even been included in conversations regarding new functionality to identify what is important to our organization.”

Terris W.

Greenlight Guru Customer

“The most helpful thing about GLG is that you don't have to worry about or be an expert on the regulations. Just follow the process, and voila, you are on your way to complying with the regs.”

Nick Punsalan, PMP

Principal Mechanical Design Engineer

On Average, Our Customers Experience:

75 %

REDUCTION IN
IMPLEMENTATION TIME

35 %

REDUCTION IN
TIME TO MARKET

50 %

REDUCTION IN TIME
SPENT ON DEVELOPMENT/DESIGN DOCUMENTATION

40 %

REDUCTION IN
NUMBER OF AUDIT FINDINGS