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No. BioIntel.io provides educational regulatory intelligence and compliance screening. All analysis output is clearly labeled as educational. We strongly recommend consulting a qualified regulatory attorney before making compliance decisions based on any analysis.

We monitor 25+ sources including FDA databases (FAERS, 510(k), BLA), ClinicalTrials.gov, PubMed/PMC, FTC enforcement actions, SEC filings, patent databases (USPTO, WIPO), venture funding platforms, and select industry publications. See our Methodology page for the full breakdown.

Signal detection runs continuously. Most government database sources are polled every 1-4 hours. The Technology Momentum Index is recalculated daily. Weekly digest reports are compiled and distributed every Monday at 8am ET.

BioIntel.io is designed for marketing compliance screening and regulatory landscape monitoring — not submission preparation. However, the signal intelligence, regulatory timeline data, and competitive landscape analysis can inform your regulatory strategy.

Claims submitted by authenticated users are stored in your personal analysis history so you can reference past results. We never share, sell, or use your claim text for any purpose other than generating your analysis. You can request deletion of your data at any time.

The TMI is a proprietary composite score (0-100) that quantifies the momentum of emerging biotech technologies. It aggregates five dimensions: research velocity (25%), clinical trial activity (25%), venture funding (20%), regulatory signals (20%), and commercial traction (10%). See our Methodology page for full details.

Yes. Enterprise plans include team management, custom alert routing, API access, dedicated account support, and volume pricing. Contact us at enterprise@biointel.io for a custom quote.

You can cancel anytime from your Dashboard under Account Settings. Your access continues through the end of the current billing period. For assistance, contact support@biointel.io.