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 Greenlight Guru Clinical 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).

Watch the webinar

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
Watch Now  

Hosted by

Páll Jóhannesson headshot

Co-founder & Managing Director,
Greenlight Guru Clinical

Chris Rush headshot1

Solutions Engineer
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.

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