“We are honored that so many bio-pharmaceutical companies have relied on ERT to support their drug development efforts, and very proud of the important role our employees play in improving patient health,” said Jim Corrigan, President and CEO of ERT.
PHILADELPHIA (PRWEB) January 09, 2020
ERT, a global data and technology company that captures critical endpoint data while minimizing uncertainty and risk in clinical trials, today announced an ERT record: 75% of the compounds approved by U.S. FDA in 2019 were developed using one or more of ERT’s eClinical solutions during the drug development process.
ERT delivers innovative imaging, cardiac safety, respiratory, and electronic Clinical Outcome Assessment (eCOA) solutions that help biopharmaceutical companies meet global regulators’ strict guidelines for demonstrating the safety and efficacy of new medical compounds. ERT’s eClinical solutions were involved in the clinical trials of 36 compounds that gained FDA approval during 2019. These compounds represent a wide spectrum of therapeutic areas, and now have the opportunity to make a big difference for patients diagnosed with various forms of cancer and rare disease, CNS and hematologic disorders, infections, and other diseases.
“We are honored that so many bio-pharmaceutical companies have relied on ERT to support their drug development efforts, and very proud of the important role our employees play in improving patient health,” said Jim Corrigan, President and CEO of ERT. “We look forward to strengthening our relationships with these global organizations and continuing to provide innovative solutions that help them develop novel treatments for patients in need.”
For more information on ERT’s suite of proven eClinical solutions, visit ert.com.
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. Since 2013, more than half 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.