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February 7, 2022

Key Pitfalls to Avoid in MedTech Clinical Data Collection

Clinical data collection is something all device manufacturers need sooner or later. And there are some common traps that are notorious for tripping up medical device companies time after time again.

Register for this free, in-depth webinar presented by clinical data experts Páll Jóhannesson and Jón Bergsteinsson from SMART-TRIAL who will help you avoid those pitfalls that make your data collection expensive, time-consuming and complex.

Watch the webinar

Greenlight Guru-SMART TRIAL Webinar 4-7-22 (1)
Specifically, this webinar will cover:
  • Paper-based data collection 
  • Avoiding the sample size calculation process
  • Collecting too much data
  • Mixing data collection methods
  • Disregarding ISO 14155:2020 & validation
  • Missing an opportunity to maximize product value
  • Dismissing ePRO/eCOA data 
  • Not taking the clinical workflow into account
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 (1)
Presenter: Páll Jóhannesson


Jón Bergsteinsson (2)
Presenter: Jón Bergsteinsson


Niki Price (1)
Moderator: Niki Price

Medical Device Guru, 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 product of Greenlight Guru.


About Greenlight Guru

Greenlight Guru is the only Medical Device Success Platform (MDSP) for companies to bring new products to market faster while simplifying regulatory compliance and reducing risk. Being the only industry specific, cloud-based software, Greenlight Guru is easier to implement, easier to use and designed to fit all medical device needs to enable innovative, safe and effective, True Quality medical devices. Visit our homepage to learn more.

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