The Challenge
Are you concerned about ensuring your clinical trials represent and serve all relevant patient populations?
Most trial designs unintentionally create participation barriers for certain demographic groups, leading to skewed data, limited research validity, and potential regulatory challenges.
Ethics committees and funding bodies increasingly require evidence that trials consider factors such as age, gender, race, ethnicity, disability, sexual orientation, and socioeconomic status.
Our EIA consultants provide comprehensive assessments based on unrivalled experience across diverse therapeutic areas and patient populations.
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...
- Identify participation barriers — We conduct thorough analyses to uncover factors that may limit participation from specific demographic groups.
- Enhance research validity — Our assessments help ensure your findings are generalizable to the full population affected by the condition.
- Ensure regulatory compliance — We help you meet evolving requirements from ethics committees and regulatory bodies regarding trial diversity.
- Support ethical obligations — We assist you in fulfilling your responsibility to ensure healthcare advances benefit all population groups.
- Provide actionable recommendations — Beyond identifying issues, we develop practical strategies to address barriers and improve inclusivity.
- Streamline ethical approval — Our pre-submission assessments help identify and address potential concerns before they delay your timeline.
- Offer ongoing monitoring — We provide frameworks for continuous evaluation throughout your trial to ensure inclusion goals are met.
- Facilitate stakeholder engagement — We connect you with advocacy groups and community representatives to enhance recruitment diversity.
