MasteScope 2.0 Simplifies Complex Clinical Trials, Enabling Investigative Sites to Focus on Patients and Data Quality
ERT, a leading global solution provider for high-quality patient safety and efficacy endpoint data collection, today announced the availability of MasterScope® 2.0, a new, comprehensive platform for spirometry, ECG, and home monitoring. Especially designed for standardized and centralized clinical trials, MasterScope 2.0 delivers an all-in-one solution that meets the data collection and processing needs of worldwide clinical trial sponsors in the development of medical treatments for respiratory conditions.
MasterScope 2.0 offers complete pulmonary function testing exceeding current ATS/ERS standards, combines home monitoring data from ERT’s AM3 family, and integrates an optional 12-lead digital ECG utilizing the ERT HES® algorithm. And, with the integration of data from third parties like the Aerocrine NIOX Mino® for collecting exhaled nitric oxide (FeNO) into the unique workflow and quality control processor, MasterScope 2.0 represents the most complete solution for clinical data collection and processing needs.
“We understand the challenges investigators face while utilizing various technologies during a complex clinical trial protocol, so we listened closely to them as we developed MasterScope 2.0,” said Achim Schuelke, Executive Vice President and Respiratory Product Line Executive at ERT. “Their feedback led to a very intuitive, appealing user interface and several new features which enable sites to better focus on the patient and the quality of their data.”
MasterScope 2.0 is the only spirometer for clinical trials that provides biometric fingerprint identification that is in compliance with the U.S. FDA’s 21 CFR 11 requirements. The system also automatically maintains a comprehensive audit trail log, facilitating quality and compliance monitoring. Additional smart features, such as the waiting room function make it easier for investigative sites to manage multiple patients on the same visit day and sophisticated procedures for automated quality checks help to improve data quality.
ERT has collected and reviewed over 3.5 million centralized spirometry measurements in more than 500 global clinical trials. To learn more about ERT’s centralized respiratory services and for more information on MasterScope 2.0, visit www.ert.com/respiratory.
Unlock Commercial Growth through Data-Driven Patient and HCP Insights
May 2nd 2025Leveraging data-driven patient and healthcare provider (HCP) insights, including social drivers of health (SDOH), is essential for life sciences companies to continuously improve patient engagement and commercial success. Mark Rodgers, AVP of Commercial Analytics at Inovalon, discusses how identifying treatment milestones, assessing HCP performance, and segmenting patient populations using SDOH data can drive targeted strategies that improve healthcare outcomes and market access
Improving Relationships and Diversifying the Site Selection Process
April 17th 2025In this episode of the Applied Clinical Trials Podcast, Liz Beatty, co-founder and chief strategy officer, Inato, discusses a number of topics around site engagement including community-based sites, the role of technology in improving site/sponsor relationships, how increased operational costs are impacting the industry, and more.
FDA Approves Nipocalimab for the Treatment of Generalized Myasthenia Gravis
April 30th 2025Approval is based on results from the pivotal Vivacity-MG3 trial in which IMAAVY (nipocalimab-aahu) demonstrated superior disease control throughout 24 weeks when compared to placebo plus standard of care.