Pricing

Simple, transparent pricing

Start free and scale as your regulatory intelligence needs grow. All plans include the educational disclaimer and core compliance features.

Starter

$0/forever

Try the platform with basic regulatory checks.

  • 5 claim analyses per month
  • Basic risk flagging
  • Educational disclaimers
  • Email support
Get Started Free
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Professional

$79/per month

Full-featured regulatory intelligence for growing teams.

  • 100 claim analyses per month
  • 10 document audits per month
  • Safer language suggestions
  • Regulatory chat assistant
  • Export reports
  • Priority support
Start Professional

Enterprise

$299/per month

Advanced compliance workflows for regulated companies.

  • Unlimited claim analyses
  • 50 document audits per month
  • SOP guardrail checks
  • Team collaboration
  • Custom checklists
  • API access
  • Dedicated account manager
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Enterprise+

Custom/annual

White-glove service for large regulatory teams.

  • Everything in Enterprise
  • Unlimited all features
  • Custom AI model tuning
  • On-premise deployment option
  • Regulatory update briefings
  • 24/7 priority support
  • Custom integrations
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Frequently asked questions

What counts as a claim analysis?

Each time you submit marketing text for regulatory risk analysis, that counts as one claim analysis. You can analyze claims of up to 5,000 characters each.

Can I upgrade or downgrade my plan?

Yes, you can change your plan at any time. Upgrades take effect immediately and downgrades apply at the end of your current billing cycle.

Is this legal advice?

No. BioIntel.io provides educational regulatory intelligence. All outputs should be reviewed by qualified regulatory counsel before making compliance decisions.

What regulations are covered?

We cover FDA biologics (351(a) BLA, 361 HCT/P under 21 CFR 1271), FTC Act Section 5, DSHEA, state-level regulations, and international frameworks. Our vault is continuously updated.

BioIntel.io provides educational regulatory intelligence only. This is not legal advice. All outputs should be reviewed by qualified regulatory counsel before making compliance decisions. Regulatory requirements vary by jurisdiction and product classification.