Regulatory-currency SaaS for clinical trials
Know when your ICF stops being current.
Upload country templates and receive passage-level alerts when laws, regulator names, retention periods, or ethics-committee language changes—complete with sourced, proposed redlines.
Built for regulatory-affairs, privacy, clinical-operations, and country-startup teams.
What to expect
Evidence before urgency.
Source-linked
Every alert points back to the authority or publication that changed.
No invented certainty
Materiality and proposed wording remain visible for qualified human review.
Country-specific
Changes are mapped to the document and jurisdiction they actually affect.
From source change to approved edit
Replace the review-date spreadsheet with a live change record.
ConsentPulse connects external regulatory change to the internal sentence it affects, so teams can review the issue instead of searching for it.
- 01
Continuous source monitoring
ConsentPulse watches laws, regulator guidance, ethics-committee templates, retention rules, and authority names across subscribed countries.
- 02
Passage-level impact analysis
Each alert points to the exact language in your ICF, privacy notice, consent language, or CTA clause that may need attention.
- 03
Review-ready redlines
Receive proposed replacement text with a clear redline, source reference, and rationale for your regulatory and legal reviewers.
Designed for the real risk
One avoided EC rejection can outweigh a year of monitoring.
Weekly
target alert cadence for relevant source changes
1 record
source, affected passage, rationale, and proposed redline
Annual subscriptions
Price the countries you need to keep current.
Final scope depends on document volume, jurisdictions, seats, and workflow requirements. Pilot pricing is confirmed before onboarding.
ICF Watch
Public intelligence
Free
Follow notable consent, privacy, and clinical-trial document changes without uploading templates.
- Public regulatory-change feed
- Selected country updates
- Plain-language change summaries
Country monitoring
Sponsor & CRO workspace
$500–$2,000 / country-seat / year
For teams that need their own templates continuously mapped against changing country requirements.
Questions before upload
A practical layer for qualified review.
Start with your highest-risk countries
Find out what changed before an ethics committee does.
Bring a sample country template and target jurisdictions. We’ll scope the monitoring set, review path, and annual pilot.