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
Regulatory affairs teams
Track your company's molecule portfolio across the authorities that matter to you, without manually checking each one.
Regulatory consultancies
Monitor across multiple clients' molecules from one place. See /partners.
Business development & market access
Get an early, sourced signal on regulatory and trial activity relevant to licensing and market-entry decisions.
Simple, flat pricing
$149/month for 2–3 authorities of your choice. No per-molecule fees. Need more authorities or seats — talk to us.