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

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Featured Capabilities:

Document Management Product Development Design Control Risk Solutions Training Management CAPA 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

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Learn valuable, career-boosting skills for the Medical Device industry. Get access to hundreds of free resources as well as subscription-based courses and certifications.

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FREE ON-DEMAND WEBINAR
June 27, 2023

How to Design the Optimal eCRF for MedTech Clinical Investigations

Designing the optimal electronic case report form (eCRF) for clinical investigations is crucial for several reasons. An eCRF plays a vital role in ensuring the accuracy, integrity, and efficiency of data collection. A well-designed eCRF contributes to the success of the clinical investigation and ultimately improves patient care by advancing medical knowledge and healthcare.

eCRFs and Electronic Data Capture are slowly becoming a standard in the MedTech industry. But collecting data in a digital manner is very different from paper.

Join Pall Johannesson, Medical Device Expert and SMART-TRIAL co-founder, to learn about the 10 top recommendations for designing electronic case report forms, including ePROs, in a medical device clinical investigation and how to ensure compliance with ISO 14155:2020 (GCP).

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Specifically, this webinar will cover:
  • Common pitfalls when designing eCRF forms
  • Key advice for designing and setting up Electronic Data Capture with eCRF/ePRO
  • ISO 14155/GCP and documentation requirements
Who should attend? 
  • Clinical Affairs and Operations professionals
  • Regulatory Affairs professionals
  • Executives and leadership involved in clinical strategy
     
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Hosted by

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Presenter:
PALL JOHANNESSON

Co-founder & Managing Director,
SMART-TRIAL by Greenlight Guru

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Moderator:
CHRIS RUSH

Solutions Engineer
Greenlight Guru

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About Greenlight Guru

Greenlight Guru is the leading cloud-based platform purpose-built for MedTech companies. The end-to-end solution goes beyond traditional QMS needs by integrating cross-functional teams, processes, and data throughout the entire product lifecycle so device makers can proactively overcome execution gaps, streamline compliance, and accelerate market success.

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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About SMART-TRIAL by Greenlignt Guru

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 page to learn more.

Since June 2022, SMART-TRIAL is a Greenlight Guru product.

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