when clinical research reflects diversity, everyone benefits
Transform your clinical research with expert patient engagement services that enhance recruitment, ensure regulatory compliance, and deliver more representative, scientifically robust results.
Are you struggling with participant recruitment, ethics committee approval, or ensuring your trials truly represent the populations you aim to serve?
Nclusiv specialises in bringing authentic patient voices into every stage of your clinical research process.
our key services
Patient Engagement: PIS/ICF Expert Reviews
Real patients review your trial documents to ensure they're truly accessible
- 10-15 day turnaround for expert patient feedback
- Condition-specific reviewers with lived experience
- Clear recommendations for improving participant understanding
patient focus groups
Collaborative sessions that amplify patient voices in research design
- Structured discussions with diverse patient groups
- Insights that enhance protocol development
- Meaningful community engagement throughout your trial
equality impact assessments
Comprehensive analysis ensuring inclusive and equitable trial design
- Identify potential barriers to diverse participation
- Regulatory compliance for ethics committees
- Data-driven strategies for enhanced inclusivity
EDI Strategy & Policy development
EDI Strategy & Policy development
Build frameworks that transform your approach to inclusive research
- Customised EDI strategies for your organisation
- Policy development and implementation support
- Demonstrate ethical leadership in clinical research
edi consulting
EDI Strategy & Policy development
edi audit & analysis
Expert guidance to integrate inclusion principles throughout your research
- Hands-on support for embedding EDI practices
- Cultural competency development for research teams
- Sustainable approaches to inclusive research
edi audit & analysis
EDI Strategy & Policy development
edi audit & analysis
Data-driven insights to strengthen inclusion and diversity practices
- Comprehensive assessment of current EDI effectiveness
- Identify gaps and improvement opportunities
- Evidence-based recommendations for enhanced inclusivity
edi staff training on protocol design
edi staff training on protocol design
edi staff training on protocol design
Build team capabilities for designing inclusive trials from the ground up
- Practical training on EDI best practices
- Protocol design skills that overcome inclusion barriers
- Create research environments where diversity thrives
Who we serve
Pharmaceutical Companies
Enhance trial diversity, accelerate recruitment, and ensure regulatory compliance with expert patient engagement services.
Contract Research Organisations (CROs)
Differentiate your offerings with proven patient-centered approaches that deliver superior trial outcomes.
Academic Research Institutions
Meet funding requirements and ethical standards while improving the scientific validity of your research.
NHS Clinical Trial Units
Access specialized EDI expertise to enhance patient engagement and trial inclusivity across your research portfolio.
