Katy Jones from Greenphire discusses how the unification of two dynamic technology solutions can increase clinical trial patent engagement and produce positive outcomes for all stakeholders, potentially improving the patient experience and shortening the overall trial length.

Learn how to overcome one of the biggest concerns in the clinical trial industry - patient recruitment. In this episode, we’ll discuss the importance of precision recruitment and site-follow up, as well as patient recruitment challenges like diagnosis, eligibility, and diversity.

Phil Lake and Dr. Kai Michael-Beeh examine the steps sponsors and study teams can take to improve data quality and reduce data variability in respiratory trials. They also discuss the innovations and trends they expect to see in the industry in the future.

Ken Faulkner and Katarina Krosback explore the potential benefits and pitfalls of Bring Your Own Device (BYOD) in eCOA clinical trials, as well as the current regulatory perspective. In this episode we discuss the future hold of BYOD, the value of patients using their own devices and the technology needed for BYOD trials.

Patricia Castellano and Emily Olsson explore how sites can benefit from developing a stronger relationship with their ABPM device vendors. They also address strategies for successful repeat ABPM sessions when a patient is non-compliant, and how ABPM achieves a type of holistic data not possible with other BP measurement methods.

The FDA has identified ambulatory blood pressure monitoring as the best option for collecting data about the relationship between blood pressure changes and therapeutic drugs. In part one of our ABPM episodes, find out how to successfully capture ABPM data and improve patient compliance.

ERT’s Drew Bustos and Dr. Santikary discuss the challenges sponsors face due to increased demands for data, and examine how modern data platforms, cloud-based technologies, and artificial intelligence can provide potential solutions when incorporated into data integration and management plans.

Are you at DIA 2019? Then tune into ERT’s best practices series for clinical trial research. In this series, we discuss the factors that determine a successful clinical trial. Topics we cover are patient engagement, data architecture, FDA guidelines, wearable devices and much more. With our expert guests, we explore how to address the many unseen obstacles of clinical research

Vivienne de Walle, Co-Founder of PT&R - a dedicated clinical trial site in the Netherlands, and Chris Porter, VP of Marketing & Digital Strategy, ERT, explore how involving clinical sites early on in the trial process can help simplify the study for sites, help sponsors avoid common, yet important, pitfalls and accelerate clinical trial timelines

ERT’s Brett Hoover and Amit Vasanji examine the massive growth trends in demand for imaging and discuss how sponsors and CROs can develop strategies and incorporate technologies that enable them to achieve better, more thorough, and less costly imaging data.