In our new whitepaper, Enhancing Recruitment and Retention in Rare Disease Trials, sponsors gain valuable insights and guidance to improve patient recruitment and retention in rare disease clinical trials.

What’s Inside:

• Utilizing patient advocacy groups and forums to effectively reach the “right” patients
• Data analysis and mining; using real world evidence for specific inclusion/exclusion criteria, patient journeys, site locations and more
• Leveraging internet, Websites and social media to inform potential patients
• Development of customized study protocols; including travel and home visit considerations

If you have any questions while reading this whitepaper or would like additional information on orphan reach’s expertise, feel free to request a consultation.