FEBRUARY 2, 2022

How to Use eConsent
Efficiently in Medical
Device Studies

The use of eConsent in medical device studies has been a topic of discussion in the medical device industry for years, and due to Covid-19, sponsors have been increasingly considering the feasibility of implementing eConsent in the clinical workflow.

Unfortunately, the time and resources required by EDC vendors to set up the solution has often been too big of a hurdle for sponsors to overcome. 

With the vision of empowering medical device manufacturers to be their best and enable all manufacturers to utilize eConsent in their clinical workflow, Greenlight Guru Clinical (formerly SMART-TRIAL) has developed a 100% autonomous and integrated eConsent solution that can be fully set up by the study sponsor.

This eliminates the costly and timely setup completely, and allows manufacturers to use eConsent in their studies when applicable. 

But how do you apply eConsent efficiently in your medical device study? Adam Steadman, and Páll Jóhannesson, present key insights on when, how and why you should use eConsent in your study. 

Watch the webinar

How to Use eConsent Efficiently in Medical Device Studies - Thumbnail
Specifically, this webinar will cover:
  • Simplified collection of informed consent and better overview
  • Flexible Consent Options
  • Better patient experience = Improved recruitment and reduced drop-out rates
  • Audit trail with full traceability
  • Improved and simplified trial process
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) 

Presenter: Adam Steadman

CCO - Americas & Asia,  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.

Since June 2022, SMART-TRIAL is a product of Greenlight Guru and has rebranded to Greenlight Guru Clinical.

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