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Medical device quality management system with document control, design controls, and CAPA for FDA-regulated companies.

Pricing

Custom quote

Founded

2013

Team size

201-500 employees

Headquarters

Indianapolis, IN

Greenlight Guru preview

Preview from greenlight.guru

At a glance

Best for

Startup (1-50), Small business (51-200), Mid-market (201-1,000), Enterprise (1,000+)

Pricing model

Custom quote

About Greenlight Guru

Greenlight Guru is a quality management and clinical evidence platform purpose-built for medical device companies. Its QMS handles document control, design controls, CAPA, risk, supplier, and audit management to support FDA/ISO 13485 compliance, while its Clinical platform supports trial data collection, PMCF, and ePRO/eCOA. It targets medtech teams that need regulatory-grade quality and clinical workflows.

Procurement & Fit

Structured facts from the vendor to help your security, finance, and procurement reviews move faster.

Trust

Security & compliance

The vendor hasn’t added security or compliance details yet.

Pricing

Commercial model

Pricing model: Custom quote

Free trial: No

Free plan: No

Contract minimum: Not specified

Procurement

Purchasing & legal

The vendor hasn’t added purchasing & legal details yet.

Fit

Best-fit company size

Startup (1-50)Small business (51-200)Mid-market (201-1,000)Enterprise (1,000+)

Buyer Fit & Positioning

Implementation & Procurement

Commercial Fit & Ecosystem

Proof, Outcomes & Momentum

Alternatives, Migration & Buyer Objections