Free FDA GMLP Glossary is a compliance software product available on the Whop marketplace, created by contraaverage and launched in May 2026.

Get a practical starting point for understanding FDA Guidance and Good Machine Learning Practice (GMLP) terminology with this free glossary for AI-enabled medical devices. This editable Word resource helps quality, regulatory, engineering, product, and compliance teams understand key terms used across governance, risk management, validation, data management, cybersecurity, transparency, post-market monitoring, and AI/ML lifecycle documentation. It is designed as a quick-reference tool for onboarding, internal alignment, and faster document review. The glossary is easy to use, easy to customize, and valuable for teams building or improving AI medical device compliance documentation. Want a more hands-on way to assess readiness? Upgrade to the FDA GMLP Compliance Checklist Package for a Word checklist and Excel tracker with pass/fail review, owners, evidence links, and audit notes. Need the full documentation system? Upgrade to the FDA GMLP Full Document Template Package for editable policies, plans, procedures, registers, matrices, and supporting templates. This glossary is not legal advice, does not guarantee compliance, and is not a substitute for legal, regulatory, clinical, or quality counsel. Not affiliated with or endorsed by the FDA or any regulator. Provided as is, with no warranty. License: single buyer license for internal business use only; no resale, redistribution, sublicensing, or sharing of the file in original or modified form.

Free FDA GMLP Glossary has offers free access.

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