The Challenge
Is your clinical research truly as inclusive as it could be? How would you know?
Many organizations believe their trials are inclusive but lack the data and analytical framework to identify hidden barriers and missed opportunities for greater diversity.
Regulatory bodies and funding agencies increasingly require evidence of EDI effectiveness, not just EDI intentions, making structured assessment essential for compliance.
Our expert audit team provides thorough, objective assessments that reveal actionable insights and clear pathways to more inclusive, scientifically robust research.
We offer a completely free introductory discussion call to address your individual needs. Sign up by filling in the quick form here:
at nclusiv we...
- Provide comprehensive assessments — Our audits examine all aspects of your research from recruitment through to data analysis, identifying both strengths and improvement opportunities.
- Analyse demographic patterns — We examine participation data to identify disparities and representation gaps across your research portfolio.
- Review policies and procedures — We assess how EDI considerations are integrated into your research governance, staffing, and organizational culture.
- Engage diverse stakeholders — We gather feedback from research participants, community organizations, and advocacy groups to understand real-world impacts.
- Develop actionable recommendations — We translate findings into practical, prioritized steps that enhance inclusion and research quality.
- Support regulatory compliance — Our assessments provide the documentation increasingly required by ethics committees and funding bodies.
- Build improvement frameworks — We establish ongoing monitoring systems that track progress and drive continuous enhancement.
- Deliver expert insights — Our auditors bring specialized experience in both clinical research and EDI principles to ensure thorough assessment.
