DECEMBER 17, 2020

eConsent in Medical Device Clinical Investigations

The age of paper has passed and eConsent is becoming an increasingly popular method to obtain informed consent in clinical investigations. The benefits of using eConsent in clinical investigations become clear to many companies as they replace outdated paper-processes.

This webinar will answer the most common questions on eConsent in medical device clinical investigations, with Jon Bergsteinsson and Pall Johannesson co-founders of SMART-TRIAL by Greenlight Guru.

Watch the webinar

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Specifically, this webinar will cover:
  • Best practices for eConsent in clinical investigations
  • The three ways of obtaining eConsent
  • GDPR compliance pitfalls when implementing eConsent
  • Answers to the most frequently asked questions about eConsent
Who Should Attend?
  • Clinical Research Professionals and Management
  • Medical Device Executives
  • Regulatory Affairs Professionals and Management
  • Quality Professionals and Management
  • Clinical Affairs Professionals and Management
  • R&D Engineers and Management
Register Now  

Hosted by

Páll Jóhannesson headshot
Presenter: Páll Jóhannesson

Managing Director, co-founder SMART-TRIAL by Greenlight Guru

Jón Bergsteinsson (2)
Presenter: Jón Bergsteinsson

Director of Sales EMEA, co-founder SMART-TRIAL by Greenlight Guru

ST-full color-big - Rune Sørensen

About Smart Trial

The only Electronic Data Capture (EDC) platform designed for Medical Devices & Diagnostics. SMART-TRIAL offers the ideal Electronic Data Capture for clinical investigations, performance studies, and PMCF/PMPF activities - including registries and surveys. SMART-TRIAL is built to empower clinical teams to be their best, and in full control of their data, without compromising on features, design, or compliance.

Visit our website to learn more.

Since June 2022, SMART-TRIAL is a Greenlight Guru product.

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