# MedPath

> Clinical trials intelligence platform for medical research professionals.

MedPath aggregates data from ClinicalTrials.gov, WHO ICTRP, EudraCT, and 12+ regulatory agencies including FDA, EMA, NMPA, TGA, and Health Canada.

## Core Features

- **Clinical Trials**: Search and analyze 500K+ clinical trials across global registries
- **Drug Intelligence**: Track drug pipelines from discovery to approval
- **Regulatory Approvals**: Monitor approvals from FDA, EMA, NMPA, TGA, Health Canada, HSA, SFDA, and more
- **AI Research**: Generate comprehensive research reports with citations
- **Company Tracking**: Track 10K+ pharmaceutical companies and their pipelines

## Key Pages

- [Home](https://atlas.medpath.com/)
- [Clinical Trials](https://atlas.medpath.com/clinical-trial)
- [Clinical Trial Search](https://atlas.medpath.com/clinical-trial/search)
- [Drug Intelligence](https://atlas.medpath.com/drug)
- [Drug Approvals](https://atlas.medpath.com/drug/approvals)
- [Organizations](https://atlas.medpath.com/organization)
- [News](https://atlas.medpath.com/news)
- [Pricing](https://atlas.medpath.com/pricing)
- [FAQ](https://atlas.medpath.com/faq)

## Data Sources

- ClinicalTrials.gov
- EU Clinical Trials Register (EU CTR)
- WHO International Clinical Trials Registry Platform (ICTRP)
- US FDA
- European Medicines Agency (EMA)
- China National Medical Products Administration (NMPA)
- Australia Therapeutic Goods Administration (TGA)
- Health Canada
- Singapore Health Sciences Authority (HSA)
- Saudi Food and Drug Authority (SFDA)
- Malaysia NPRA
- Philippines FDA
- Kenya PPB
- Spain CIMA-AEMPS
- UK EMC

## API

MedPath provides a structured API for programmatic access to clinical trial data, drug intelligence, and regulatory approvals.

## Contact

For questions or partnerships, visit [https://atlas.medpath.com/faq](https://atlas.medpath.com/faq).