Continuously monitor global regulatory filings, clinical trials, pricing, and pipeline activity with 99.5% accurate, verified intelligence.
The Problem
Monitor global regulatory filings and clinical trials with normalized, verified data from every major healthcare authority.
Track cross-pharmacy pricing and pipeline changes with standardized, real-time intelligence across every source.
Access verified healthcare market intelligence without costly enterprise contracts or long-term commitments.
The Data Product
Every regulatory filing, trial update, pricing move, and provider directory record carries the verifier ID, the timestamp, and the source URL. Point-in-time captures preserved, with no retroactive adjustment.
FDA, EMA, MHRA, PMDA, CDSCO drug approvals, indication changes, safety communications, black box warnings, orphan drug and breakthrough designations, warning letters, drug shortage notices.
Sample Data
Every signal includes its source, timestamp, verifier, and audit trail—ensuring complete transparency and traceability.
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{
"signal_id": "FDA-2026-NDA-215432",
"signal_type": "drug_approval",
"regulator": "US Food and Drug Administration (FDA)",
"brand_name": "Zephrex",
"generic_name": "sotinemab",
"applicant": "Corvus Pharmaceuticals",
"therapeutic_class": "oncology",
"indication": "third-line HER2-positive metastatic breast cancer",
"approval_type": "NDA_original",
"approval_date": "2026-07-15T00:00:00Z",
"approval_pathway": ["Priority Review", "Breakthrough Therapy Designation"]
}Sources & Coverage
Compliance-first
Every source we monitor is publicly available. No hospital records, no claims data, no patient information ever ingested.
Zero Protected Health Information. Public regulatory, clinical trial, and pricing data only.
Delivery infrastructure, contracts, and processes designed to complement your HIPAA program without triggering PHI handling.
Every record traces to its source URL and capture timestamp. Point-in-time captures preserved. Audit trail on demand.
Who it's for
Track FDA, EMA, MHRA, PMDA, and CDSCO filings continuously. Approval notifications, safety communications, and enforcement actions routed to your regulatory queue. Point-in-time snapshots for audit trails.
Monitor competitive pipelines, formulary movements, PBM decisions, and cross-pharmacy pricing. Correlate against your therapeutic area to catch competitor launches, indication expansions, and pricing moves early.
Track clinical trial phase transitions, sponsor moves, enrollment updates, and endpoint changes across ClinicalTrials.gov, EU CTR, and WHO ICTRP. Competitive trial landscape maintained continuously.
Pipeline signals, regulatory approvals, and clinical trial updates on your watchlist companies. Structured, timestamped, delivered before market open. Point-in-time captures for backtesting.
Cross-pharmacy drug pricing, formulary intelligence, and specialty drug tracking. Verified pricing that stands up under employee benefits review.
How It Works
The engine continuously watches any web source you name. Portals, marketplaces, PDFs, filings, review sites, ad libraries. Configurable per industry, per source, per cadence. Durable workflows that survive failure and keep running.
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AI classifies every observed change. Price movement, new listings, structural change, sentiment shift, filings, launches. Every classification carries a confidence score. Low-confidence records route to human review. Verified accuracy runs at 99.5% at the field level, with verifier ID and timestamp on every record.
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Detected signals join your live data. Your CRM, your warehouse, other Crawlify streams. Cross-signal correlation surfaces composite events. A price drop plus a new ad campaign plus a PDP rewrite reads as one repositioning signal, not three unrelated alerts.
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Signals become actions. REST API, webhooks, warehouse writes, CRM updates, workflow triggers, Slack routing. On your schedule, in your systems, source-traceable end to end.
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How It Compares
| Capability | Cortellispharma intelligence | Citelinepipeline | Evaluate Pharmamarket intelligence | Crawlify |
|---|---|---|---|---|
| FDA regulatory monitoring | Yes | Yes | Yes | Yes |
| International regulatory (EMA, MHRA, PMDA, CDSCO) | Yes | Yes | Partial | Yes |
| Clinical trial intelligence | Yes | Yes | Partial | Yes |
| Drug pricing & market access | Limited | Limited | Yes | Yes |
| Provider directories & HCP intelligence | No | No | No | Yes |
| Point-in-time captures preserved | Limited | Limited | Limited | Yes |
| Per-record provenance (verifier ID + timestamp) | No | No | No | 99.5% SLA |
| Delivery (Snowflake, S3, REST, webhooks) | Limited | Limited | Limited | Yes |
| Mid-Market Pricing | Yes | Yes | Yes | Yes |
| Pricing shape | Enterprise annual | Enterprise annual | Enterprise annual | Scoped to your source list and refresh frequency. Talk to us |
Use Cases
A benefits consultant serving mid-market employers tracks specialty drug pricing across six major pharmacy retailers plus PBM formulary movements. Verified pricing data delivered daily. Employer clients receive quarterly benchmarking reports with per-record source URLs, meeting fiduciary duty documentation requirements.
An oncology biotech tracks phase transitions and enrollment updates across 40+ competitor trials in HER2-positive breast cancer. Signals arrive in the strategy team's Notion workspace with point-in-time snapshots preserved. Competitive intelligence briefings updated weekly with verified data.
A generics manufacturer monitors FDA orange book patent listings, Paragraph IV certifications, and approval decisions across 200+ molecules. Signals routed to the regulatory affairs team via Salesforce. Point-in-time snapshots archived for patent litigation documentation.
Five main categories: regulatory filings and approvals (FDA, EMA, MHRA, PMDA, CDSCO), clinical trial intelligence (ClinicalTrials.gov, EU CTR, WHO ICTRP, CTRI, ISRCTN), drug pipeline and competitive launches, drug pricing and market access, and HCP and provider directories. If you need a category we don't currently monitor, ask and we'll assess it.
Working in one of the industries we're building for? Talk to us about how the engine can be tuned to your signals.
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