Learn how our unrivaled combination of patient and investigator data helps guide study design, site selection, patient recruitment and study conduct.

Let’s meet to explore customized solutions to help speed your drug development process.
1.  Stop by Booth #1921 (and enter to win an Apple Watch!)
Explore our interactive kiosks to learn how our proprietary solutions help you to:

  • Identify eligible patients and ideal sites for faster patient recruitment 
  • Incorporate patient intelligence into protocol design
  • Proactively identify and mitigate study risks
  • Gain operational efficiency with flexible, scalable clinical trial service delivery

3.   Join us at our Innovation Theater Presentation
Tuesday, June 25 | 9:45 – 10:15 a.m.
Fixing the Patient Recruitment “Leaky Funnel”

Kate Garretson Reese, MPH
Executive Director, Site and Patient Centricity
Covance Inc.  

Michelle Jones, MSc
Senior Director, Data and Technology Organization
Covance Inc.
4.   Attend our Session Presentations and Panel Discussion
Monday, June 24 | 3:30 – 4:30 p.m.
Using Appropriate Count-Based Statistical Models for KPIs, Risk Metrics, QTLs, etc.

Michael Farnum, PhD, MS
Sr. Director, Informatics
Covance Inc. 
Tuesday, June 25 | 8:00 – 9:15 a.m.
Panel Discussion
Personalized Healthcare and Clinical Outcomes: How Real World Endpoints Can Improve Approval and Access to Medicine?

Gillis Carrigan, PhD
Epidemiologist, Director, Market Access  
Covance Inc. 
Tuesday, June 25 | 2:00 – 3:15 p.m.
Making Pediatric Clinical Trials Fun (and Easy?): Virtualization, Wearables and Other Technologies Utilized in Clinical Trials

Gina Calarco, MPH, BSN, RN, CCRC
Director, Rare Disease and Pediatrics
Covance Inc.

Wednesday, June 26 | 2:00 – 3:15 p.m.
Statistical Models of Risk Flux Reveal Dynamics of RBM-Managed Clinical Trials

Kristin Stallcup, MP, PMP
Sr. Director, Informatics
Covance Inc.
We look forward to seeing you at DIA 2019!

Covance respects your Privacy.
Manage your Subscriptions.
© Copyright 2019 Covance Inc. All rights reserved.