WEBINARS

• Transforming Oncology Trials With Next-Gen eCOA

  With the FDA stating last fall that the “patient’s voice” is key to understanding real-world-impacts, eCOAs and ePROs are becoming quintessential tools for cancer trials.

• The Top 5 Myths About eCOAs In 2025

  Join leading clinical experts as they debunk the top 5 myths about eCOA in 2025, separating fact from fiction to help clinical operations, procurement, and data management teams make smarter decisions.

• Reduce Patient And Site Burden Through Excellence In Trial Logistics

  Watch for an insightful webinar where you’ll explore the latest strategies and innovations for managing clinical trial operations with a focus on device provisioning and data workflows.

• Defining And Implementing The Right Oncology Digital Strategy

  A panel of oncology experts shares how top life science companies are using a combination of DHTs, ePROs, clinical trial platforms, and more to ease oncology research and drastically reduce timelines.

• Maximize Control And Transparency On The Path To Study Go-Live

  Simplify the historically complicated, black-box processes around eCOA solution deployment, content storage and visualization, and global go-live.

• The New Era Of Evidence Generation In Clinical Trials

  Learn how top pharmaceutical companies are using novel innovations to drive greater speed, scale, and access in clinical research than ever before in this webinar hosted by Musaddiq Khan, Vice President of DCT Solutions at Medable.

• Harnessing The Potential Of Patient-Level Data In Clinical Trials  

  Join our panel of industry leaders as they explore innovative methods and best practices for incorporating fully consented patient data in clinical trials.

• Technology Overload: Addressing Site Challenges Of Digital Trials

  Watch as speakers explore the experiences of sites conducting digital and hybrid trials, discussing the critical benefits of a change management strategy and a unified digital trial platform.

• Amplifying Evidence With Unified Clinical Trial Data Collection

  In this presentation, we explore the transformative potential of integrating a unified clinical trial data collection platform with intelligent automation, challenging the inadequacies of the status quo.

• What It Really Takes To Adopt eConsent Across Large Pharma

  Explore the benefits of incorporating consent management technology and discover practical strategies for developing effective change management and training programs.

• Enhancing The Clinical Trial Experience With Consumerization

  Clinical trial technology has transformed the ways we can engage patients. Learn from experts at Uber Health and clinical tech companies how you can supercharge the patient experience with consumerization.

• Keeping Up With ClinOps: Why And How To Improve Delivery

  Industry experts discuss the concept of a trial platform as a service and how it can accelerate and enhance the day-to-day functions of clinical operations throughout the entire lifecycle of a study.

• Enhancing Oncology Clinical Trials Through The Use Of Digital Technologies

  The most difficult clinical research just became more challenging. Learn tactics on how teams can simplify oncology research while solving new and old issues.

• Everything You Need To Know About Adopting eConsent Across Large Pharma Organizations

  Did you know that the average cost for a delayed trial is between $600,000 and $8 million per day? Discover how electronic consent management technology is helping sponsors, CROs, and sites.

• Deploying A Unified Framework To Accelerate Recruitment And Reduce Timelines

  Learn how and why unified platforms are effective at delivering better patient access and shortening clinical trial timelines with this webinar.

• The Digital Future Is Now

  Discover best practices and see real examples of how top pharmaceutical companies like GSK, Syneos, and others successfully drive the transformation of clinical development to achieve higher patient engagement and retention using digital technologies, all while emphasizing a foundational platform approach for their future trials.

• How Technology Can Alleviate Patient Burden In Oncology Trials

  Hear from young cancer survivor Dr. Lindsay Matt, and Medable SMEs as they document what challenges patients face in clinical trials, and how to help alleviate them with modern technology.

• The Platform Shift is Here: Are you Realizing ROI Across your Portfolio of Studies?

  Research shows that the global DCT market will reach $14B by 2026. Research also suggests that up to 90% of clinical trials are at risk of failure. Faulty trial designs, patient retention, costs and flawed data collection are drivers for the failure rate in clinical trials. The risks of study failure are reduced by taking a patient- first enterprise platform approach.

• Digital Versus Digitized: Common Misconceptions About eConsent

  In this on-demand webinar attendees will learn about the common misconceptions surrounding eConsent, as well as the benefits they can realize through a digitally-enabled approach.

• Everything You Need To Know About Hybrid/Decentralized Trials

  This webinar provides insight into an understanding of hybrid and decentralized clinical trials (DCT), the facts and fiction around decentralized trials, and why decentralized trials are not an all or nothing approach.

• Agile eConsent: Taking A Flexible Approach To Global Implementation

  Hear from industry experts on how they successfully combined agile eConsent technology with global regulatory expertise to increase enrollment rates and reduce both site and patient burden.

• Enable Next-Generation Clinical Research At Scale

  In this webinar, Medable SMEs take you through the end-to-end process of conducting decentralized clinical research, including benefits, common pitfalls and challenges, and more. 

• Accelerate Time To Target Endpoint In Cardiometabolic Studies Using Patient-Centered Technology Solutions

  In this webinar, industry experts share their perspectives on how to address drug development challenges within cardiometabolic clinical studies and provide input on the impact of new regulatory guidance such as the DEPICT Act.

• Three Data Trends to Consider Now When Developing Your Decentralized Clinical Trial Strategy

  In this free webinar, learn how to update your clinical data strategy that ensures you can scale trials globally while decreasing the overall burden on sites and patients.

• Collect Better Oncology Trial Data, Easier

  In this webinar, experts discuss how enriching oncology clinical trials with RWD generates deeper insights and improves operational efficiency to achieve better patient outcomes.

• The New Vaccine Race: Why A Decentralized Approach Wins

  What does it take to get vaccine trials up and running quickly and efficiently? As it turns out, the best answer is DCT. Learn why in the available webinar.