Summary: Labcorp has launched Labcorp Global Trial Connect, a suite of central laboratory solutions designed to enhance the speed and efficiency of clinical trials by streamlining investigator site workflows.

Takeaways:

  1. Labcorp Global Trial Connect aims to simplify investigator workflows, enhance patient experiences, and accelerate the market introduction of therapies.
  2. The suite offers digital and data solutions to improve study startup efficiency, maintain momentum, and increase throughput.
  3. Key features include site enablement resources, supply readiness support, and comprehensive study management and investigator support.

Labcorp announced the launch of Labcorp Global Trial Connect, a suite of central laboratory solutions aimed at increasing the speed of clinical trials where the heart of clinical research is conducted: investigator sites.

“The patient-investigator-biopharma sponsor relationship is at the foundation of a successful clinical trial. Global Trial Connect simplifies the investigator workflow, improves the patient experience and ultimately enables biopharma sponsors to bring therapies to market faster,” says Jon DiVincenzo, EVP and president, Central Laboratories and International at Labcorp.  “As the world’s leading central laboratory, Labcorp is dedicated to improving the pace of clinical trials focusing on the investigator site experience from study initiation to patient recruitment and data collection.”

Further reading: Labcorp Announces New Strategic Service Offerings in Precision Oncology Portfolio

About Labcorp Global Trial Connect

Labcorp Global Trial Connect, available to current Labcorp Central Laboratory clients, incorporates complementary digital and data solutions that help accelerate clinical study startup, maintain study momentum, and increase study throughput. Capabilities include:

  • Site enablement resources to identify new study opportunities, enhance patient access and recruitment and improve diversity in clinical trials.
  • Supply readiness support to increase study startup efficiencies, reduce trial delays and reduce supply and kit waste.
  • Site workflow facilitation to help integrate sample collection and tracking data, provide visibility and actionable analytics to both sites and sponsors, and reduce errors, queries, holds and data revisions through eRequisition functionality.
  • Study management and investigator support to accelerate study startup and maintain study momentum with 24/7 site support and on-demand tools and trainings.

Photo: iStock Editorial via Getty Images.