Key Pitfalls to Avoid in MedTech Clinical Data Collection

FREE ON-DEMAND WEBINAR

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

Hosted by

Presenter: Páll Jóhannesson

CEO, SMART-TRIAL

Presenter: Jón Bergsteinsson

CCO - EMEA, SMART-TRIAL

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 their website to learn more.

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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