DECEMBER 2, 2021

How to Collect PMCF Data for Lower Class Devices & WETs

Designing PMCF activities for lower class medical devices and other well-established technologies can be a challenge.

Most users aren‘t interested in being involved in long or dreadful clinical investigations. So for those devices used on a day-to-day basis in clinical practice, we need to implement modern methods to gather data on clinical experience and safety.  

In this webinar, Greenlight Guru Clinical (formerly SMART-TRIAL)‘s PMCF expert, Jon Bergsteinsson, teams up with CEO of Evnia, Efstathios Vassiliadis, to present you with a simple, yet powerful tool, to collect real world clinical experience data to use in your PMCF report.

Watch the webinar

How to collect PMCF data for lower class devices and WETs - thumbnail
Specifically, this webinar will cover:
  • The importance of PMCF for lower-class devices and WETs
  • How to optimize PMCF processes
  • Which PMCF activities to prioritize
  • Data collection tips for PMCF
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

Presenter: Efstathios Vassiliadis

CEO, Evnia

Jón Bergsteinsson (2)
Presenter: Jón Bergsteinsson

Co-founder, Greenlight Guru Clinical


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.

Evnia logo

About Evnia

Evnia's goal is to accelerate innovation in the medical industry in order to bring significant changes to the quality of care and life for patients. They are a company of like-minded professionals who have unique expertise that enables them to provide a holistic approach to regulatory compliance in the field of medical devices and in vitro diagnostics.

Visit their homepage to learn more.

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