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Enterprise Layer Intelligence
Categories/Legal Tech/Rhizome AI
Rhizome AI

Rhizome AI

Founded by https://www.linkedin.com/in/chemishra/

Always know what the FDA thinks

Pricing model

Paid

Rating

★ People love it

Time to value

Immediate

You can use Rhizome to search through 2.5TB of FDA documents and regulatory databases to get instant answers to compliance questions. It references up to 1,000 documents from public health authority databases across 6 markets including FDA, EMA, and other regulatory bodies. Each answer includes direct citations to specific pages in authoritative sources, helping regulatory professionals research guidance documents, clinical trials data, and safety reporting requirements without spending weeks on manual research.

What Rhizome AI does

Search FDA databases for specific regulatory guidanceGenerate compliance reports with cited sourcesCompare regulatory requirements across different marketsResearch clinical trial protocol requirementsFind regulatory precedents for product approvalsVerify safety reporting timelines and formatsResearch labeling and packaging requirementsCheck post-marketing study obligationsSearch across 2.5TB of regulatory documentsReference up to 1,000 documents per answerDirect citations to specific page numbersZero hallucinations reported in 2025Covers FDA, EMA and 4 other regulatory regionsAccess to premarket and postmarket databasesClinical trials and guidance documents includedFine-tuned AI with inference-time accuracy checks

Pricing breakdown

Pricing model: Paid

PlanList price
Project$400 / mo
Professional (paid yearly)$3,500 / yr total
Business (paid yearly)$20,000 / yr total

Tutorials & Demos

Frequently asked

Web-based Interface, REST API (Enterprise only), Veeva Vault (Unverified), SharePoint (Unverified)

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Rhizome, FDA regulatory research, compliance databases, regulatory affairs, pharmaceutical guidance, medical device regulations, clinical trials research, regulatory documentation, health authority databases, EMA guidelines