6 essential steps to ensure MDR compliance before May 2021
A recent report surveying representatives from the medical device industry across the world found that more than 55%…
How MedRhythms Captures Clinical Efficacy Data with Castor
Using Decentralized Trial Technology to Ensure Study Continuity and Data Quality During COVID-19 and Beyond
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.
How to manage your study in Castor
During this webinar, we showed how to efficiently manage studies in Castor. This includes: How to add users…
5 steps to meet PMCF requirements
Read the white paper to learn how Castor’s 5-step approach to PMCF can be used to fulfill MDR requirements.
Tips & Tricks for data entry in Castor EDC
This webinar is dedicated to data entry users of Castor EDC. If you are conducting data entry for…
Satisfying PMCF requirements by utilizing IIS data
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.
How to Ensure Compliant Data in a World Where Protocol Deviations Are the New Normal
In 2020, the SARS-CoV-2 coronavirus has infected millions and resulted in death for hundreds of thousands. It has…
All you need to know about randomization in Castor
This webinar teaches everything you need to know about randomization in Castor. This includes: How to randomize records…