Resource Library

When the COVID-19 pandemic began, the industry needed to focus immediately on research continuity and determine how to mitigate the impact on clinical trials while protecting participant safety.

The path to market for medical devices can be fraught with obstacles. One of the first challenges confronted…

Medical research data holds the key to solving the world’s greatest healthcare challenges. It is therefore, one of…

A recent report surveying representatives from the medical device industry across the world found that more than 55%…

Download this white paper to learn why patient-centric, remote research technologies such as eConsent, EDC, and ePRO are critical during COVID-19 and beyond.

During this webinar, we showed how to efficiently manage studies in Castor. This includes: How to add users…

Read the white paper to learn how Castor’s 5-step approach to PMCF can be used to fulfill MDR requirements.

This webinar is dedicated to data entry users of Castor EDC. If you are conducting data entry for…

This white paper describes an approach that would enable medical device manufacturers to leverage anonymous data from IIS projects to support the fulfilment of PMCF data requirements.