Global Compliance Infrastructure

Autonomous disclosure
intelligence for
clinical trials

Disclosed. Verified. Done.
Replace manual compliance chaos with a single system that monitors, prepares, redacts, and posts across every global registry. Not faster spreadsheets. No spreadsheets at all.
Request Demo
The Problem

Billions in pharmaceutical value held hostage by spreadsheets

Trial results sit in email threads. Disclosure deadlines pass in silence. Regulators issue fines that were entirely preventable. This is not a workflow problem. It is an infrastructure failure.
Manual Processes
Compliance by Spreadsheet
Teams track deadlines across multiple registries using Excel. Human error is inevitable. Regulatory risk is constant.
Fragmented Systems
No Single Source of Truth
Data lives in silos. CSRs, protocols, amendments — scattered across departments. Disclosure becomes archaeology.
Regulatory Complexity
Global Requirements Multiply
ClinicalTrials.gov, EudraCT, CTIS, ISRCTN — each with unique formats, deadlines, and redaction rules. Compliance teams drown.
The Solution

Not a service. An operating system for disclosure.

Product
Global Registry Sync™
Automated multi-registry publication engine. ClinicalTrials.gov, EudraCT, CTIS, ISRCTN — one submission, every jurisdiction.
Product
Intelligent Anonymization Protocol
AI-powered PII and CCI detection with context-aware redaction. Maintains scientific integrity while ensuring privacy compliance.
Product
Compliance Horizon™
Predictive deadline intelligence across all regulatory bodies. Not reminders — a real-time regulatory threat map.
Product
TrialCore Extract
Structured data liberation from Clinical Study Reports. PDFs in, registry-ready datasets out.
Product
ClearSignal™
Regulation-compliant lay summaries generated at clinical accuracy. EU CTR Article 37 ready.
Product
AuditShield
Continuous compliance posture monitoring. Every action logged, every decision traceable, every inspector satisfied.
Why clinicmeta

Built for pharmaceutical infrastructure, not healthcare IT

Regulatory-First Architecture
Every feature designed around global disclosure requirements. Not adapted from generic project management tools.
Autonomous Intelligence
The system monitors, prepares, and executes. Your team reviews and approves. Compliance becomes supervision, not execution.
Enterprise Security
SOC 2 Type II certified. GDPR compliant. Data residency options for every jurisdiction. Built for pharma's security requirements.
Get Started

Ready to eliminate compliance chaos?

Schedule a demo to see how clinicmeta transforms disclosure from a compliance burden into an automated infrastructure layer.
Request Demo