Research Partnerships & Institutional Collaboration
Join FibroNex in advancing fibromyalgia research with ethics-grade data infrastructure.
What FibroNex offers research partners
Ethics-Ready Infrastructure
UK GDPR compliant, versioned consent management, and k-anonymity protection built in. Designed to meet NHS and university ethics board requirements.
Structured Longitudinal Data
Daily symptom logs, medication tracking, and validated questionnaires (FIQ, PHQ-9, GAD-7). Checkpoint reports at months 1, 3, 6, 9, and 12.
Patient Cohort Access
Connect with consented participants for clinical studies. Separate study-specific consent workflow and pseudonymised data exports.
White-Label Ready
Platform can be branded for institutional use. API access, custom questionnaires, and integration with existing research infrastructure.
Partnership opportunities
Universities & Research Institutions
Collaborate on clinical trials, observational studies, or longitudinal research. Access anonymised datasets with full ethics compliance.
NHS Trusts & Clinical Services
Pilot FibroNex as a patient-reported outcome measure (PROM) tool. Clinician-ready reports integrate with existing care pathways.
Pharmaceutical & Medical Device Companies
Real-world evidence (RWE) data collection for clinical development, post-market surveillance, or patient registry studies.
Technical & ethical standards
Data Protection
- UK GDPR Article 9 compliant (special category data)
- Row-level security on all patient data
- Pseudonymisation and k-anonymity (k≥5)
- Cryptographic signing of reports
- EU-region hosting (Vercel + Supabase)
Research Ethics
- Versioned consent with withdrawal tracking
- Participant Information Sheets (PIS) provided
- Separate service and research consent
- Complete audit trail for compliance
- Right to data export and deletion (GDPR)
Register institutional interest
Your information will be used solely to discuss research partnership opportunities. We respect institutional privacy and will not share your details without permission.