Our Patients Deserve to Be Seen
Parkinson's disease affects millions across our continent, yet Africa contributes less than 1% of global research data.
This means clinical trials exclude our populations. Treatment protocols ignore our genetics. Disease patterns in our communities remain invisible to the world.
PMAN changes this story. Together, we're building a repository that ensures our patients are seen, counted, and represented.
Simple Steps, Lasting Impact
Join a growing community of African clinicians making history.
Register & Verify
Join the network with your institutional credentials. Your account is verified for data integrity.
Record Patient Data
Use standardized questionnaires and assessment scales during patient visits.
Contribute to Research
Anonymized, aggregated data feeds into continental research initiatives.
Built for African Clinicians
Every feature designed with our unique healthcare realities in mind.
Standardized Assessments
MDS-UPDRS, Hoehn & Yahr, and other validated scales built directly into your workflow.
Data Security
End-to-end encryption, role-based access, and complete audit trails for every action.
Works Anywhere
Responsive design works on any device, optimized for varying connectivity conditions.
Export & Report
Generate reports and export data in research-ready formats with one click.
Multi-Site Support
Collaborate across institutions while maintaining complete data ownership.
Africa-First Design
Built for African healthcare contexts and infrastructure realities.
Your Data, Our Sacred Trust
Patient privacy is paramount. We implement the highest security standards to protect the communities we serve.
- 256-bit AES encryption at rest and in transit
- Role-based access control
- Complete audit logging
- Data anonymization for research exports
- International data protection compliance
Let's Connect
Questions about PMAN? Want to bring your institution into the network? We'd love to hear from you.