See Approve Suite in two minutes
Everything the FDA, the SEC and ClinicalTrials.gov publish, in one feed, filtered to the companies, therapeutic areas and regulations you name.
The free plan needs no card. Pro adds your watchlist, a daily email, instant alerts and Ask AI from $79 a month. See pricing
The full product
Approve Suite is an AI regulatory platform for biotech quality and regulatory teams. It reads public FDA, SEC and ClinicalTrials.gov records on a schedule, summarizes each new record and says why it matters, matches it against the companies, indications, CFR parts and GxP areas on your watchlist, and delivers the matches in one daily email, with instant alerts for critical items. Ask AI answers your questions about any company, trial or regulation from the same records and cites the events it used. Every item links to its primary source.
- Your watchlist. Companies, indications, CFR parts, GxP areas and keywords. Each match says which of your rules it hit and why it matters.
- One email a day. A digest at the hour you pick, and instant alerts on critical events within about fifteen minutes.
- Company explorer and profiles. Trial track record, FDA record, financials and fundraising for about 11,400 companies.
- Ask AI. Questions answered from the product's own data, with the events it used cited.
Informational only. Not regulatory, legal, or medical advice. Every item links to its public source.
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