- LabCorp launches fully integrated clinical trial platform to streamline the drug development process featuring.
- The new clinical trial platform will deliver dramatic reductions in patient and study site administrative tasks, improve trial resiliency, and maintain study continuity through the use of the company’s data, technology, and direct-to-patient outreach capabilities.
Global life sciences company LabCorp today announced new capabilities that will transform the clinical trial experience with the goal of streamlining the drug development process. This transformation will enable LabCorp’s drug development business, Covance, a global leader in decentralized clinical trials (DCTs), to quickly and efficiently connect patients to clinical trials, which will allow for better access to potential drugs, vaccines, and medical devices. Additionally, the seamless, tech-enabled, patient-centric capabilities will provide a better clinical trial experience for patients, and biopharmaceutical and medical device customers.
LabCorp now offers a comprehensive and fully-integrated patient, site, and customer experience for DCTs. The clinical trial platform will deliver dramatic reductions in patient and study site administrative tasks, improve trial resiliency, and maintain study continuity through the use of the company’s data, technology, and direct-to-patient outreach capabilities. These results are made possible through the recent acquisitions of GlobalCare, a global mobile nursing and ambulant care organization that provides services in more than 65 countries, and snapIoT, a global medical technology company that provides a digitized clinical platform (mClinical) that supports remote participation in clinical trials.
Streamlining the Drug Development Process
The company’s innovative digitized clinical trials solution provides data interoperability across the trial delivery continuum and optimizes the site workflow by reducing the number of disparate tools and platforms used during clinical trials to one integrated solution. This solution could include functions such as eConsent, ePRO, and eCOA; telehealth and connected devices to improve data collection; and digitization of mobile nursing visits and sample collections to accelerate benefits of DCT, namely faster enrollment, easier engagement, more efficient studies, and quicker data locks.
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Improved Clinical Trial Design
A hallmark of this new approach is that LabCorp can now speed up trial design and implementation while de-risking the execution process by providing complete, integrated solutions from a single partner. LabCorp’s services include improved trial design that takes into account its Voice of the Patient and direct-to-patient recruitment strategies; virtual offerings, such as telemedicine to enable more efficient doctor-patient interactions; access to LabCorp’s approximately 2,000 patient service centers; mobile phlebotomy and nursing services; and other clinical trial services the company offers. All of these services and technologies are supported by a high-touch patient contact center and can be delivered by one provider, LabCorp and its drug development business, Covance.
“By deploying protocol-specific, tech-enabled solutions, we are providing patient-centric trial experiences,” said Dr. Paul Kirchgraber, CEO, LabCorp’s drug development business, Covance. “In addition to reducing the burden on patients, our approach improves data quality and provides operational efficiencies that will benefit our biopharmaceutical and medical device customers.”
Source: News Break
