Why This Matters
Parkinson's disease affects millions across Africa, yet the continent contributes less than 1% of global research data.
Clinical trials rarely include African populations. Treatment protocols aren't tailored to local genetics. Disease patterns remain undocumented.
PMAN changes this by creating a unified, standardized repository ensuring African patients are represented in global research.
African populations systematically underrepresented in research.
Treatment guidelines don't account for local factors.
Disease progression data remains unknown.
How It Works
Three steps to contributing to groundbreaking research.
Join the network with your institutional credentials. Your account is verified for data integrity.
Use standardized questionnaires and assessment scales during patient visits.
Anonymized, aggregated data feeds into continental research initiatives.
Features
Every feature designed with African healthcare realities in mind.
MDS-UPDRS, Hoehn & Yahr, and other validated scales built directly into your workflow.
End-to-end encryption, role-based access, and complete audit trails for every action.
Responsive design works on any device, optimized for varying connectivity conditions.
Generate reports and export data in research-ready formats with one click.
Collaborate across institutions while maintaining complete data ownership.
Built for African healthcare contexts and infrastructure realities.
Security
Hospital-grade security measures ensure patient privacy and regulatory compliance.
Contact
Questions about PMAN? Want to learn how your institution can participate?