Medical Devices

AKRN Scientific Consulting, a medical device CRO, used Castor’s flexible EDC solution to handle constant mid-study changes for their client.

Castor’s eSource platform streamlined collecting, capturing & processing large amounts of clinical data to train AusculThing’s AI algorithm.

When the pandemic hit, Julius Clinical was passionate to help in the global fight against COVID-19 and excited to expand on its experience with Decentralized Clinical Trials (DCT).

Researchers are looking to incorporate remote technologies into medical device trials for a wide range of device classifications. This article explores current regulations for various classes of medical devices and how this will impact the need for participants to visit research sites throughout the trial.

In today’s rapidly evolving regulatory landscape, ensuring medical device safety and performance goes beyond the approval phase. Effective…

Registry studies focused on a specific medical device are a valuable tool to capture the safety and outcomes of the device over its lifetime. Read more here.

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.