Medical Device Industry

In the wake of Brexit, medical device companies secure a UKCA mark as proof of conformity to place their device on the UK market. Learn what this means for your organization and how to prepare.

The following is an excerpt from our free whitepaper ‘Satisfying PMCF requirements by utilizing IIS data’. Click here…

eClinical systems must be flexible and adaptable to keep up with the ever-changing demands of modern clinical trials….

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…

CEOs of medical device companies have an intuitive sense of what they need from their clinical data. However,…