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

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82% Respond that they are Implementing Elements of virtual Trials due to the Pandemic.

Key Learnings from ERT's Industry Survey on Virtual Trial Trends

"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," Jim Mahon, VP, Chief Strategy Officer, ERT

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.

According to the survey, which was conducted by ERT in April and May, 2020:

  • The biggest issue keeping participants up at night is screening for new clinical trials patients (79%)
  • The primary issues impacting trials over the next six to twelve months are trial management (32%) and patient recruitment and enrollment (25%)
  • The most common ways to collect data in a virtual clinical trial are telehealth (75%) and patient-used devices (75%)

“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.

About ERT
ERT is a global data and technology company that minimizes uncertainty and risk in clinical trials so that its customers can move ahead with confidence. With nearly 50 years of clinical and therapeutic experience, ERT balances knowledge of what works with a vision for what’s next, so it can adapt without compromising standards.

Powered by the company’s EXPERT® technology platform, ERT’s solutions enhance trial oversight, enable site optimization, increase patient engagement and measure the efficacy of new clinical treatments while ensuring patient safety. In 2019, 75% of all FDA drug approvals came from ERT-supported studies. Pharma companies, biotechs and CROs have relied on ERT solutions across 15,000 studies, spanning more than four million patients to date. By identifying trial risks before they become problems, ERT enables customers to bring clinical treatments to patients quickly ─ and with confidence.

For more information, go to ert.com or follow us on LinkedIn and Twitter.

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Christine Tobin
ERT
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