This guide offers a clear-eyed perspective on the current eCOA landscape, providing sponsors with actionable guidance to make confident, informed vendor choices.

This ebook describes how electronic clinical outcomes assessments (eCOA), mobile digital assessments, and other innovative data capture technologies are able to “meet patients where they are” in Parkinson’s Disease trials – with increasingly objective, sensitive, and continuous measures. 

Explore the creation and implementation of the electronic versions of COAs (eCOAs) on a high priority study with a new client.

Master protocol design trials require an endless stream of consent forms, adding time, cost, and risk. Learn how a feature-rich eConsent platform can simplify those processes and improve engagement.

Watch this webinar to see the latest eConsent workflow from recruitment, to pre-screening, to remote consent.

Despite the challenges associated with large volumes of data, maintaining quality and regulatory compliance, and enhancing patient engagement, the solutions for managing them can be simple and efficient.

Explore four of the 15 system functionality considerations highlighted in an eCOA Consortium article that aim to create a more thorough and standardized approach to ePROM implementation.

Learn how digital solutions can contribute to a more participant-centered approach and potentially enhance the regulatory utility of PRO data while improving the overall quality and efficiency of oncology trials.

The Bring Your Own Device (BYOD) model, supported by Trialkit, is an innovative approach in clinical trials that allows participants to use personal smartphones or tablets for data collection.