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 The benefits of using eConsent in clinical investigations become clear to many companies as they replace outdated paper-processes.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 Greenlight Guru Clinical (formerly SMART-TRIAL).

Watch the webinar

LinkedIn Promotion - eConsent
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 Greenlight Guru Clinical (formerly SMART-TRIAL)

Jón Bergsteinsson (2)
Presenter: Jón Bergsteinsson

Director of Sales EMEA, co-founder Greenlight Guru Clinical (formerly SMART-TRIAL) 


About Greenlight Guru Clinical

Greenlight Guru Clinical is the leading clinical data collection toolbox, purposefully built for MedTech. Collect and manage clinical data in pre and post-market clinical studies, including registries, cohorts, surveys, human factor testing, design validation, and more.

Greenlight Guru Clinical meets the regulatory requirements of the FDA, EU, and most other countries, and ensures compliance out-of-the-box with GCP and ISO 14155:2020.

Visit our website to learn more.

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