Webinars

Panel Discussion: Harnessing the Potential of Patient-Level data in Clinical Trials     

The use of patient-level datasets in clinical trials can improve the accuracy of trial findings and streamline decision making. Join our panel of industry leaders as they outline innovative methods and best practice for implementing fully consented patient data in clinical trials, as well as the difference value driven data and digital healthcare can make.  

webinar patients as partners clinical trial
Webinars

Optimizing Digital Evidence Generation Using the Patient’s Lens

Uncover how Medable drives success by leveraging patient-centric insights and eCOA technology to enhance data quality/compliance, diversity, and retention in clinical trials.

Webinars

Demo On Demand: eCOA+, patient & site experiences, and pulse oximeter sensor

eCOA
6 min

VP of Solution Consulting, Jess Dolphi, showcases a few of the platform’s features, including site experience, patient experience, data and oversight dashboards, and a demonstration of connecting a pulse oximeter sensor for remote data capture.

Webinars

Bringing empathy into the digital environment

Learn best practices to incorporate empathy and human interaction in the digital environment with attentive listening, building relationships with sites, promoting clinical trial technology implementation, and learning from other industries that have successfully transitioned to digital.

webinar DCT clinical trials
Webinars

Last Year’s DCT Is Today’s Clinical Trial

DCTs have transformed from a disruptive force challenging the norm to an integral concept, now widely embraced in the clinical trial landscape. Join us for this upcoming Clinical Leader Live session, where experts will explore the current landscape, highlighting the positive impact of DCTs and their transition from innovation to indispensable practice in the era of evidence generation and modern clinical trials.

Webinars

Ethical Review of Decentralized Clinical Trials (DCTs): Tools, Resources & Best Practices

IRB
6 min

Industry experts from Medable and Harvard School of Medicine discuss how to equip your future digital/decentralized trial IRB & ethics submissions for success.

Webinars

Amplifying Evidence with Unified Clinical Trial Data Collection

eCOA
6 min

Join us for a discussion about how combining a unified clinical trial data collection platform with intelligent automation can revolutionize drug development and why the current status quo is no longer sufficient. With novel capabilities, the industry can now explore new possibilities, such as incorporating additional sensors to identify surrogate or alternative endpoints, rethinking adaptive trial designs, and quickly responding to emerging data.

Webinars

Keeping up with ClinOps: Why and how to improve delivery

Medable is joined by Join GSK and Lightship for a panel discussion on how a trial platform as a service can enhance, expedite, and improve the day-to-day operations of clinical operations across the life cycle of a study.  

Webinars

Optimizing Evidence and Design Using the Patient’s Lens

Uncover how to work with patients to shape everything from protocols to data collection.

Webinars

Technology Overload: Addressing Site Challenges of Digital Trials

Katie madden, Digital & Process Optimization at GSK, joins Medable’s Andrew MacKinnon and Annie Hesslewood to discuss the importance of implementing a change management strategy coupled with a unified digital trial platform that streamlines eConsent, eCOA, sensors, and integration workflows into a single end-to-end experience.

Webinars

Unlocking Patient Engagement: Enhancing the Clinical Trial Experience with Consumerization

In this panel discussion, industry experts from Uber Health, iXlayer, and Medable will discuss the rise in technology adoption has also raised the expectations of trial participants, who now seek simpler, more consumer-like experiences in clinical design.

Webinars

DCT Digital Week: Creating the Digital Foundation for Scale in Clinical Development

Learn how sponsors and CROs can improve their clinical trial conduct by developing new strategies that create sustainable, repeatable, and effective clinical conduct.

See how Medable can make your trials more efficient.