Developments, news and strategies for drug development specific to phase I through Phase III global clinical trial management, execution, project management and outsourcing. Go→
News, articles and issues specific to clinical trial practice and implementation at the investigative site level. Go→
Strategies and innovations related to how clinical professionals are utilizing technology internal and external to their organizations to advance clinical trials. Go→
News, articles and issues specific to laboratories role in the clinical trial, including ECG, imaging, genotyping, tissue samples and more. Go→
News, developments and strategies for clinical trials conduct in relation to the FDA, EMEA and other global regulatory authorities overseeing the drug development industry. Go→
News, articles and strategies related to clinical trial design which impact postmarketing studies, therapeutic areas, adaptive trials, statistics, protocols and more. Go→
ERT, a leading global solution provider for high-quality patient safety and efficacy endpoint data collection, today announced an expansion to its comprehensive suite of electronic Clinical Outcome Assessment (eCOA) data collection solutions for use in clinical trials. With this expansion, clinical trial sponsors can improve trial efficiencies while reliably collecting important eCOA data via patients’ personal Apple® (iOS) or Android™ phones and tablets.
An extension of ERT’s flagship DIARYpro® solution, the Bring Your Own Device (BYOD) option is based on over 25 years of scientifically and regulatory-proven COA data collection experience. This native mobile application enables trial sponsors to acquire high-quality eCOA data while eliminating the cost and time associated with purchasing, shipping, and managing a global fleet of dedicated eCOA devices. In addition, ERT’s BYOD solution ensures that assessments are presented consistently across different device types and screen resolutions.
“DIARYpro has set the industry standard for high data quality and reliability,” said Bob Young, EVP and Product Line Executive, eCOA at ERT. “In expanding the solution to include a BYOD option, we conducted significant research among global clinical trial sponsors to ensure it not only meets these standards, but also offers valuable features that will streamline the eCOA data collection process.”
Unlike other mobile applications that run within web browsers and require a live internet connection, ERT’s BYOD solution allows fully-offline operation for when data must be entered during strict time windows, regardless of internet connectivity. Further, on-device reminders to begin or continue assessments are not dependent on any external email or text server, and these notifications blend naturally into smartphone users’ daily lives, enhancing compliance.
Having supported over 1,200 COA global clinical trials to date, ERT’s solutions and services are routinely relied upon by biopharmaceutical researchers for capturing important patient data during clinical development. For more information on ERT’s comprehensive suite of eCOA data collection solutions, including BYOD, visit www.ert.com/eCOA.