Regulatory changes, caught at the source.
RegWatch monitors official regulatory authority sources and flags changes that affect your molecules — regulatory actions, clinical trials, research, and news.
No card required · Free for 14 days
Currently monitoring live
Full list with live status and last-checked times on /coverage.
Regulatory teams track many authorities by hand.
Checking each regulator's site, clinical trial registries, and the literature for every molecule in a portfolio doesn't scale — and a missed labeling change or trial status update has real consequences.
Illustrative example — not live customer data
- regulatory
Label update filed
FDA · 2 days ago
- trial
Phase 3 status changed to Recruiting
ClinicalTrials.gov · 5 days ago
- research
New publication indexed
PubMed · 1 week ago
How it works
Monitor
RegWatch checks official authority sources on a schedule — regulator databases, clinical trial registries, and biomedical literature.
Extract
New or changed items are pulled from each source and normalized: title, date, authority, and a link back to the original document.
Classify
Each item is tagged by type (regulatory, trial, research, news) and given a verification tier based on how directly it traces to an official source.
Alert
Genuinely new items surface on your dashboard and in your "what's new" feed — never a re-notification of something you've already seen.
Who it's for
Business development & market access
Get an early, sourced signal on regulatory and trial activity relevant to licensing and market-entry decisions.
Regulatory consultancies
Monitor across multiple clients' molecules from one place. See /partners.
Regulatory affairs teams
Track your company's molecule portfolio across the authorities that matter to you, without manually checking each one.
Simple, flat pricing
$500/month for 2–3 authorities of your choice. No per-molecule fees. Need more authorities or seats — talk to us.