Ethical & Regulatory Standards
Our commitment to ethical data practices and regulatory compliance in health research and surveillance.
Core Ethical Principles
Informed Consent
All data collection adheres to informed consent principles, with clear communication about how data will be used.
Data Minimization
Only necessary data is collected and retained, limiting exposure and enhancing privacy protection.
Privacy by Design
Privacy considerations are embedded into every stage of data infrastructure and research design.
Fair Use
Data is used equitably for public health benefit, with safeguards against misuse or discrimination.
Regulatory Frameworks
EU GDPR
General Data Protection Regulation compliance for data processing involving EU partners.
Key Requirements
- Lawful basis for processing
- Data subject rights
- Cross-border transfer safeguards
Gouvernance des donnees de l'UA
Alignment with AU frameworks on data governance and digital transformation.
Key Requirements
- Data sovereignty principles
- Regional cooperation
- Capacity building
National Health Data Laws
Compliance with health data regulations in each participating country.
Key Requirements
- Country-specific requirements
- NPHI oversight
- Local ethics approvals
Processus de Revue Ethique
Initial Assessment
All research proposals undergo initial ethical screening to identify potential concerns.
Ethics Committee Review
Proposals are reviewed by the EpiScientia Ethics Committee and relevant national ethics boards.
Approval & Conditions
Approved projects receive ethical clearance with any specific conditions for data handling.
Ongoing Monitoring
Continuous monitoring ensures compliance throughout the project lifecycle.
For questions about ethical standards or to submit a research proposal for review:
Contact Ethics Committee