Overcoming Challenges in Implementing eConsent in Clinical Trials

Life Sciences, Clinical Trials, Patient Recruitment & Retention,
  • Wednesday, January 24, 2024

In this insightful webinar, discover how electronic informed consent (eConsent) revolutionizes clinical trials through compliance, inclusivity, security, comprehension and engagement for participant-centered processes. eConsent has emerged as a pivotal advancement in the clinical trial industry, revolutionizing the traditional paper-based consent process and making participation possible for previously unreachable populations and patient demographics.

This webinar offers a wide-ranging exploration of relevant regulatory compliance, as well as digital inclusivity, data security, participant comprehension and engagement strategies — all vital components in ensuring a seamless and participant-centric eConsent process.

The featured speaker will cover the following topics:

  • Navigating regulatory compliance
  • Bridging the digital divide
  • Securing eConsent processes
  • Confirming participant comprehension
  • Fostering participant engagement

Attendees will also learn practical knowledge to navigate the complex landscape of eConsent implementation, fostering a smoother and more participant-centric informed consent process in clinical trials.

Join this webinar to discover the potential of participant-centered clinical trials through the diverse insights of eConsent, revolutionizing compliance, inclusivity, security, comprehension and engagement strategies.


Greg Tullo, Viedoc

Greg Tullo, Vice President of Professional Services Americas, Viedoc

Greg Tullo is the Vice President of Professional Services (PS) for the Americas at Viedoc. He has over 15 years of experience encompassing time at the National Institutes of Health (NIH), CROs and tech start-ups. Now, Greg oversees professional services at Viedoc across the Americas and regularly demonstrates Viedoc’s suite of clinical solutions to prospective clients and assists current clients by ensuring that they maximize the benefit they receive by using Viedoc.

Message Presenter

Who Should Attend?

This webinar will appeal to Executives, Directors, Managers and Department Heads working within:

  • Clinical data management
  • Clinical operations
  • Clinical research organizations (CRO)
  • Biotechnology industry strategy
  • Sponsors
  • Data security and privacy
  • Regulatory affairs

What You Will Learn

Attendees will gain insights into:

  • Practical knowledge to navigate the complex landscape of eConsent implementation
  • Regulatory compliance, digital inclusivity, data security, participant comprehension and engagement strategies
  • Knowledge of a smoother, participant-centric, informed consent process in the dynamic and evolving realm of clinical trials

Xtalks Partner


Viedoc Technologies designs engaging software that modernizes clinical research so that necessary treatments can reach the people who need them faster. We accomplish this by combining technology and creative design to streamline, automate, and simplify conventional processes within clinical research. Founded in 2003, Viedoc Technologies has become a leader in Electronic Data Capture (EDC), offering full support for decentralized clinical trials, unrivaled setup times, high-level security measures, and global support.

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