Don’t forget to check out our sessions prepared by our Medable thought leaders.

Check out the session details below: 

Keynote panel

"When Will DCT 2.0 Be Here?" 

Speaker:

  • Michelle Longmire, CEO, Medable

DCT Spotlight Panel Town Hall 

Speakers:‍

  • Michelle Longmire, CEO, Medable
  • MaryAnne Rizk, Chief Strategy Officer, Medable

Medable team at CNS

Michelle Longmire - Speaker
CEO, Medable

MaryAnne Rizk - Speaker
Chief Strategy Officer

Ravi Ramachandran
SVP, General Manager, Enablement

Stan Beaumont
Senior Director, Business Development

Taylor Ronan
Senior Director, Business Development

Joe Dustin
‍VP & General Manager of eCOA

Keynote panel

“The Next Evolution of Study Delivery: Shifting the paradigm to bringing trials into the community”

Speakers: ‍

  • Michelle Longmire, CEO, Medable
  • ‍Jamie Macdonald, CEO, Parexel
  • Najat Khan, Head Data Science, Janssen
Keynote panel

“Real World Evidence” 

Speakers:

  • MaryAnne Rizk, Chief Strategy Officer, Medable
  • Jean Drouin, CEO, Clarify Health
  • Jamie Macdonald, CEO, Parexel
  • Tony Clapsis, SVP & General Manager, CVS Health Clinical Trial Services

Interested in scheduling a meeting with us at CNS Summit?

Fill out the form to book some time.

Expand Global Access to Trials

Accessible on any web-enabled device (BYOD or provisioned), our scalable solution can inform and consent participants anywhere in the world. Flexible enough for any country or site, you can easily collect compliant signatures (digital or wet-ink), on-site or remote with integrated TeleVisit.

Improve Participant Retention

Deliver an engaging, informational experience for your participants and their caregivers with an easy-to-follow web-based app, featuring explainer videos, interactive diagrams, optional self-assessments and more.

Minimize Compliance Errors

Gain complete visibility and oversight into your trial with real-time monitoring of all consent activities within a single dashboard and ensure inspection-ready audit trails with fully integrated template management and version control.

Self-service authoring tool to easily create engaging consent templates

Biosample attribution to confirm storage permissions for consent objects

Permission-based workflows by roles and responsibilities for secure control

Compliant with FDA 21 CFR Part 11, eIDAS, HIPAA, GDPR, and ICH GCP

Andrew Mackinnon

Vice President and General Manager eConsent and Digital Solutions

Designed by Trial Experts

Our team of experts will partner with you to determine the best approach for your unique consent needs. Schedule a call to learn more about our scalable, web-enabled tools to level up your consent process.

Schedule Consultation