Open Data & Global Regulatory Portal | Eunoia Health
Live Telemetry Active: Connected to ClinicalTrials.gov REST API & Global Regulatory Frameworks.
Eunoia Health Logo Beta v1.0
AI-Assisted Asset Repurposing Engine

Live Clinical Telemetry & Global Regulatory Intelligence

Aggregating real-time data feeds from ClinicalTrials.gov, OpenFDA, and international regulatory bodies worldwide to scout, normalize, and revitalize stalled therapeutic candidates.

Active API Feeds

Live

Monitored Registries

450k+ Studies

Primary Target

Phase I/II Stalled

Global Scope

Worldwide Agencies

Real-time Ingestion

Stalled & Terminated Trial Radar

Direct API stream pulling recent non-active trials for secondary indication evaluation.

NCT ID / Title Sponsor Conditions Status Action
Connecting to ClinicalTrials.gov REST API…
International Harmonization

Global Regulatory Authority Integration Matrix

Comprehensive tracking across major international health authorities and oversight jurisdictions worldwide.

North America

Active Feed
  • US FDA (United States) OpenFDA / IND
  • Health Canada (Canada) CTDB / DPD

Europe & United Kingdom

Active Feed
  • EMA / CTIS (European Union) CTR / EudraCT
  • UK MHRA (United Kingdom) ILAP Pipeline
  • Swissmedic (Switzerland) HPC / Authorizations

Asia-Pacific (APAC)

Active Feed
  • Japan PMDA (Japan) Sakigake / JAPIC
  • China NMPA / CDE (China) CDE Registry
  • Australia TGA (Australia) CTN / CTA Scheme
  • South Korea MFDS (South Korea) K-FDA Approvals
  • Singapore HSA (Singapore) TP Register

Latin America

Active Feed
  • ANVISA (Brazil) Sanitary Registry
  • COFEPRIS (Mexico) Protocol Approvals

Africa & Middle East (Excluding Regional Restrictions)

Active Feed
  • Saudi SFDA (Saudi Arabia) Clinical Registry
  • SAHPRA (South Africa) Reliance Pathways
  • African Medicines Agency (AMA) / AVAREG Harmonized AU Network
Discovery Pipeline

How Eunoia Health Revitalizes IP

Converting unmined raw outputs into structured commercial clinical assets.

1. Automated Scouting

Continuous algorithms screen open databases and global regulatory registries for molecules with established Phase I safety profiles that lacked targeted secondary efficacy.

2. FAIR Normalization

Raw assay deposits and clinical logs are parsed and formatted into standard CDISC/SDTM schemas, ensuring complete data interoperability and audit readiness.

3. Matchmaking & CRO Trial

Repurposing dossiers are published to biopharma sponsors and research institutes to initiate accelerated, cost-effective Phase II proof-of-concept trials.

Open Data Vault Intake

Deposit Dataset or Nominate Stalled IP

Submissions route directly to 02_Open_Data_Portal_Submissions Vault