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More than a Quality Management System: Tools for the entire MedTech Lifecycle.

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Featured Capabilities:

Document Management Training Management Product Development Design Control Risk Management CAPA Management Audit Management

Experience the #1 QMS software for medical device companies first-hand. Click through an interactive demo.

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Data collection and management designed for MedTech clinical trials.

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Featured Capabilities:

Electronic Data Capture (EDC) Electronic Case Report Forms (eCRF) Electronic Patient Reported Outcomes (ePRO) Ad-Hoc Data Collection (Cases) Post-Market Surveys Product Add-Ons

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Ultimate Guide to Comparing Quality Management System Solutions

This eBook compares the best QMS software solutions to help medical device companies make an informed decision when investing in a quality management system.

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ON-DEMAND WEBINAR
April 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 Greenlight Guru Clinical 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

Managing Director, Greenlight Guru Clinical

Jón Bergsteinsson (2)
Presenter: Jón Bergsteinsson

Co-founder - Greenlight Guru Clinical

Niki Price (1)
Moderator: Niki Price

Medical Device Guru, Greenlight Guru

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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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About Greenlight Guru

Greenlight Guru is the leading connected, cloud-based platform purpose-built for MedTech companies. The end-to-end solution streamlines product development, quality management, and clinical data management by integrating cross-functional teams, processes, and data throughout the entire product lifecycle.

Greenlight Guru’s platform is used by organizations across the globe that are replacing their disjointed, legacy tools and solutions to bring life-changing products to people faster and with less risk.

Visit our homepage to learn more.

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