Medable

See how AI agents will transform your trials.


Agentic AI is rewriting how trials get done. Come see what's possible and what agents leading sponsors are already putting to work.

  • Study builds in weeks instead of months with agentic eCOA.
  • CRAs getting hours back every week via our Clinical Monitoring Agent.
  • TMF Agent that keeps you inspection-ready.

Top-20 pharma is running on these agents today.

Book time with our team at Booth #33151 to see the agents live and talk through what they could do for your oncology portfolio.

 

  • McCormick Place Convention Center, Chicago, IL
  • Booth #33151
  • May 29-June 2

Book a meeting

Schedule a meeting or demo with our platform experts at our DIA booth.

Reserve a 1:1

Skip the line; book time with our team in advance.

Meet the Medable team

Come by booth #to talk with one of our clinical research and trial experts.
Chief Executive Officer
Michelle Longmire
Discuss recent and current research on DCTs and current state of novel clinical trial methodologies.

Chief Revenue Officer
Dave Orrico
Discuss your DCT and enterprise solutions for pharma and biotech.

VP DCT Solutions
Musaddiq Khan
Medable’s expert on therapeutic area solutions and oncology trial deployment.

Chief Medical Officer
Pamela Tenaerts
Discuss recent and current research on DCTs and current state of novel clinical trial methodologies.

Executive GM, Customer Value
Andrew Mackinnon
Discuss on eConsent, Site adoption AI, and the latest Duke University Base Lab pilot study results.

VP ADOPTION & CHANGE MANAGEMENT
Camila Matheny
Discuss effective strategies to implement digital trials for your studies.
Senior Vice President, Enterprise Sales
Joe Mele
Discuss your DCT and enterprise solutions for pharma and biotech.
Senior Vice President, Enterprise Sales
Tyler Pugsley
Discuss your DCT and enterprise solutions for pharma and biotech.

Intersection of Innovative Development Models and Investment Approaches That Move the Needle at the Portfolio Level

New to SCOPE 2024 - we bring together for the first time, a business-focused panel of strategics from the pharma, investor, healthcare, CRO, and technology start-up communities, to discuss partnership models that drive much needed innovation in clinical trials and impact development at the portfolio level. In this panel we will address the following questions:
  • How can Pharma manage risks and investments while continuing to remain at the forefront of drug development, clinical research, and trial technology?
  • What alternative business models and risk-sharing partnership can support innovation, in a resource constrained environment?
  • Where are the opportunities and the ROI from such partnerships?
  • What emerging technologies are showing growth and investment and are moving the needle in clinical research?
  • TBD
  • Tuesday, February 13
  • 3:30 PM EST
  • 30 minutes
FEB

13

Michelle Longmire
MEDABLE
Co-Founder and CEO

Angela DeLuca
TAKEDA
Vice President, Head of Oncology & Cell Therapies Clinical Operations, Global Development Office, R&D

Michael Greeley
Flare Capital Partners
Co-Founder & General Partner, Healthcare Technology

The New Frontier:
How Intelligent Automation is Transforming Clinical Deployment

Join us as Colin Weller, GM, Evidence Generation Platform at Medable, unveils how intelligent automation technology reduces clinical trial deployment timelines and accelerates evidence generation at scale as shown in their latest results to reduce trial deployment timelines by 50%. Weller will discuss how Top-10 global pharmaceutical companies are benefiting from Medable’s novel technology, and how the expanded use of digital measures and biomarkers will continue to accelerate clinical development timelines.
  • TBD
  • Tuesday, February 13
  • 8:30 AM EST
  • 30 minutes
FEB

13

Colin Weller
MEDABLE
General Manager, Platform
Pamela Tenaerts
MEDABLE
Chief Scientific Officer
Special Guest
TBA
TBA

SESSION HIGHLIGHT

Responsibility and Oversight in Decentralized Clinical Trials

Join Medable’s CSO, Pamela Tenaerts to discuss issues that drive principal investigator (PI) oversight and responsibility in modern clinical trials where research and data gathering activities are no longer confined to the traditional site model.
Wed, June 28 | 10:30-11:30am

ROUNDTABLE DISCUSSION

RWD: Maximizing Value and Quality through End-to-End Patient Centricity

Join Medable’s VP, Digital Transformation Strategy, Reem Yunis and Walgreen’s Head, Digital Optimization, RWE Clinical Trials, Kendal Whitlock for a follow up roundtable discussion tied to session: Real-World Data: Maximizing Value and Quality through End-to-End Patient Centricity.
Wed, June 28 | 1:15-2:15pm
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