Medical Device Industry

Post-market surveillance (also known as Post-Marketing Surveillance or PMS) refers to the requirement that manufacturers monitor their medical…

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.

Download this guide to learn how to incorporating an Electronic Data Capture (EDC) system in your medical or diagnostics device trials.

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

Join this webinar to understand how eConsent works, where it falls in the regulatory guidelines & see a practical demonstration of eConsent software.

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…

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