Patient Insights Program
The life science industry frequently uses patient centricity as a buzzword, but promoting the idea of patient centricity without action dilutes the term’s meaning and frustrates patients. Patients are the end-users of clinical trial solutions, and the best experiences for patients ultimately bring the most value for everyone involved in running clinical trials.
Medidata’s Patient Insights program infuses the patient perspective into the software development life cycle to create technical solutions that improve the overall patient experience in clinical research operations.
Generate Better Patient Experience
Sponsors / CROs
Engage patients through Medidata’s Patient Insights Program and apply design thinking methodologies to influence better trial designs and solutions. Through Medidata’s Patient Insights Program, we do the heavy lifting to provide actionable insights and recommendations to improve your patients’ clinical trial experiences, diversity, and inclusion.
Patient Insights improves the site experience by lowering the execution burden through optimized trial design. This ultimately improves patient retention rates due to a better patient experience.
Key Features of Patient Insights
Patient Insights Board
The Patient Insights Board is a team of patient advocates, experts across numerous therapeutic areas and medical journeys. They guide Medidata with input, insights, and feedback on the patient experience for our products and initiatives.
Through the Patient Insights Program, you gain access to insights generated from this extraordinary team.
Patient Design Studios
Patient Design Studios are innovative workshops with our Patient Insights Board Members and other Patient Cloud team members in multi-day face to face sessions or single day virtualized workshops to guide the creation of protocols and patient-facing solutions.
eCOA provides a flexible, intuitive model for capturing patient data that is designed to make it easier for patients to engage in clinical trials. Built as part of the unified Medidata platform, eCOA improves your study experience with flexible deployment options, a groundbreaking global instrument library, and dedicated services and support.
Supporting both onsite and remote consent, Medidata eConsent is proven to be a superior learning tool for patients. Our regulatory and IRB-approved process automates patient review of study materials and provides better tools for connecting sites and patients. Patient consent data is fully integrated with Rave EDC, further streamlining the enrollment process.
Medidata Sensor Cloud delivers a more complete picture of the patient experience while allowing for greater flexibility throughout clinical trials. Our common model enables rapid ingestion, standardization, and analysis of data from any device resulting in greater clinical insights that can deliver more effective treatments and ultimately new therapies for patients.
How Are You Ensuring Patient Centricity?
See how the Patient Insights Program can help you truly deliver patient-centric solutions and trial designs, enabling a better experience for patients, sponsors, and sites.
Making Clinical Research Better for Patients with Patient Centricity by Design
Access our latest white paper which details this ground-breaking Patient Centricity by Design (PCbD) program, and how it can advance the science of clinical research and bring new therapies more quickly to those who need them.
How Patient Insights are Changing Trial Solutions
Pharmaphorum interviews Anthony Costello on his perspective on using Patient Insights in trial design, and how Medidata is putting this process into effect in order to deliver patient-centric solutions.
Patient Centricity Beyond the Hype
Tune into this 5-part snackable video series discussing patient centricity with Alicia Staley, VP of Patient Engagement at Medidata and a cystic fibrosis patient, and Takeda representatives to hear about their perspectives on what it means to deliver patient-centricity.