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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…

In 2020, the SARS-CoV-2 coronavirus has infected millions and resulted in death for hundreds of thousands. It has…

Last updated on June 30, 2020 For existing and new Castor customers Castor will continue to deliver its…

Bas is one of our Senior Software Engineers. Having recently joined our team of Castorians, I wondered how…

Through the Medical Device Regulation (MDR) and new version of ISO 14155, the regulatory landscape for clinical investigations with…

Introduction The implementation of the new EU Medical Device Regulation (MDR) just got a plot twist: COVID-19. This…

The ongoing COVID-19 pandemic is one of the most serious health crises in modern history, affecting an unprecedented…

Clinical trials are experiencing significant disruption worldwide due to the COVID-19 pandemic. Medical research is not immune to…

As of early April 2020, over 1,000,000 people have been confirmed infected with the SARS-CoV-2 coronavirus, and governments…