ERT Survey Indicates Swift Adoption of Virtual Clinical Trials Due to COVID-19

ERT, the global leader in clinical endpoints data collection, today announced the results of a recent industry survey that indicate an acceleration in the adoption of virtual clinical trials due to the COVID-19 pandemic. According to the survey report, ‘Virtual Trials and the COVID-19 Pandemic: The State of the Industry,” 82% of clinical trial professionals polled stated that their organizations are incorporating virtual trial technologies due to the pandemic.

Government imposed stay-at-home orders have posed a challenge to clinical trial sponsors and contract research organizations (CROs) as traditionally, clinical trials revolve around patients’ physical access to investigative sites. An alternative to this is the virtual clinical trials paradigm in which patients are at the center of new medical product development and elements of the process such as screening, visits, and data transmission are managed electronically from remote locations.

 

“There are many benefits to virtual clinical trials,” said Jim Mahon, Vice President, Chief Strategy and Marketing Officer, ERT. “They are safer and more convenient for patients and more cost-effective for sponsors and CROs. Patient recruitment is easier, drop-out rates are lower, timeframes are shorter, and endpoint data is more accurate. The acceleration we’re seeing in the adoption of virtual clinical trials is a net positive for all stakeholders. It allows for the continuation of critical studies during COVID-19, and more patient-focused and efficient studies post-pandemic. We look forward to witnessing how these powerful technologies impact the availability of life-changing therapies and treatments.”

Download the report, “Virtual Trials and the COVID-19 Pandemic: The State of the Industry,” including detailed survey findings and analysis, at virtualtrials.ert.com.

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