Webinars

eCOA Digital Week: An honest assessment of eCOAs from a site perspective

eCOA
6 min

Joe Dustin, VP/GM of eCOA and Annie Hesslewood, Site & Patient adoption lead at Medable host an open discussion with a panel of sites and CRAs to provide a candid assessment of how upcoming changes in the eCOA landscape can reduce burden on participants and sites to maximize the chance of success in clinical trials.

Webinars

Leverage novel options in oncology clinical trial design to reduce burden for patients and sites

eCOA
6 min

Flo Mowlem, Senior Director, eCOA Science & Solutions shares insights on how electronic solutions, with a focus on patient-reported outcome (ePROs) can reduce burden on participants and sites to maximize the chance of success in oncology clinical trials.

Webinars

How to supercharge real world evidence generation in Phase IV trials

Experts from Medable, Syneos, and Pluto Health discuss how they have partnered to deploy patient-first digital trial solutions that leverage RWD, transforming it into actionable RWE insights for a sponsor client.

Webinars

What it really takes to adopt eConsent across large pharma

Learn about the benefits of adopting consent management technology and best practices around developing change management and training programs to help sponsors, CROs and sites get the most out of eConsent.

Webinars

The digital future is now

Watch the on-demand panel discussion between Medable, Syneos, Illingworth and Veeva, moderated by Gilead, as they discuss how the next generation of clinical development is now.

Webinars

Deploying a patient-first framework to accelerate recruitment & reduce overall trial timelines

eCOA
6 min

Learn how to utilize digital data-flow designs in clinical trials to improve patient diversity and inclusion, increase operational efficiencies, enhance patient enrollment, engagement, and retention, and realize financial value.

Webinars

The platform shift is here: Are you realizing ROI across your portfolio of studies?

Join Medable's Mohammed Ali, Chief Domain Expert and Shubha Govil, SVP of Product Management,Platform to hear how top pharma teams have adopted digital technology across a platform to reduce costs and accelerate time to market.

Webinars

The importance of quality in the informed consent process

Join Aditum Bio's Shayanne Ali and Medable's Andrew Mackinnon, as they discuss the most common issues with the paper-based consent process, and what to look for in a complete consent management solution in order to reduce quality issues while improving oversight.

ecoa person image
Webinars

Actionable data: How to deploy & use patient-centric data collection to improve patient experiences & sharpen decision making

eCOA
6 min

Medable's Gillian Livock, SVP/GM Digital Solutions and Sean Connelly, SVP, Product Management, join Antoine Pivron, Head of Health Solutions EMEA at Withings, to discuss the industry's move toward patient-first data collection, how to increase operational efficiencies, enhancing the patient experience in clinical trials using data, and how to use data insights to drive key decision-making.

Webinars

ePROs: Transforming oncology research

eCOA
6 min

In this webinar, VP of Digital Trial Solutions Musaddiq Khan, VP of Product Strategy Colin Weller, and Cancer Survivor Lindsey Matt discuss how Medable is supporting a patient-first approach in complex Oncology clinical trials

Webinars

Building trust between clinical trial stakeholders through a DCT framework

Industry experts from Pfizer, Advarra, and Medable showcase how to design a framework of decentralized offerings that provide greater ease of use, effectiveness, and flexibility for sites for every type of research setting; decentralized/hybrid, virtual, or in-person. In addition, they discuss how DCT solutions and site partners are creating an impact to improve diversity and access while optimizing clinical research for patients.

Webinars

Digital vs digitized: Common myths about eConsent for clinical trials

Alex Burrington, CTI Principal of Vertex, and Andrew Mckinnon, VP, GM of eConsent discuss common myths around eConsent, how to improve comprehension with patient-centric consent, and how to use a digital consent management tool to improve trial compliance, quality, and oversight.

See how Medable can make your trials more efficient.