With Covid-19 Halting Clinical Trials, Wearables Could be Key — But Data ‘Wild West’ Gets in the Way Date Published: Aug 11, 2020 Article Before the COVID-19 pandemic, leveraging digital technologies in medical product development seemed impossible with the industry’s patient recruitment, timeline, and success rate struggles. However the global lockdown forced researchers to reconsider, forever changing how clinical trials are conducted. For the first time ever, pharmaceutical and technology companies collaborated to develop common study standards and protocols. But this is just the start. Find out why this collaboration needs to continue to improve clinical trials beyond the pandemic. Read More Share: LinkedInTweet Recommended Resources Article Conversation with Bill Byrom & Mariana Fontana: Measuring Aspects of Health in Heart Failure Research Dr. Bill Byrom, Principal, eCOA Science at Signant Health, recently had the pleasure of sitting downwith Professor Marianna Fontana, Professor... Download Now Article Conversation with Bill Byrom & Julian Gillmore: Increasing the Usefulness of COAs in Heart Failure Research Dr. Bill Byrom, Principal, eCOA Science at Signant Health, recently had the pleasure of sitting downwith Professor Julian Gillmore, Professor... Download Now Article Optimal COA Measurement Strategy in Modern Oncology Trials The inclusion of patient-reported outcomes (PRO) data in oncology medication labeling in the U.S. has been comparatively limited. Recent FDA... Read Now