Blog articles25 May 2021 Post-Market Surveillance (PMS): What You Need to Know and Do Now Post-market surveillance (also known as Post-Marketing Surveillance or PMS) refers to the requirement that manufacturers monitor their medical… Learn more
Blog articles19 November 2020 UKCA Mark: The Impact of Brexit on Medical Devices and 7 Steps to Prepare 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. Learn more
Blog articles5 October 2020 Common shortcomings of clinical research data for PMCF The following is an excerpt from our free whitepaper ‘Satisfying PMCF requirements by utilizing IIS data’. Click here… Learn more
Blog articles6 August 2020 5 Ways to Make Your Clinical Trials More Efficient With the Castor API eClinical systems must be flexible and adaptable to keep up with the ever-changing demands of modern clinical trials…. Learn more
Blog articles29 July 2020 What Will Trial Enrollment & Engagement Look Like in a Socially-Distanced World? 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. Learn more
Blog articles24 July 2020 Jumpstart Your Medical Device Preclinical Phase The path to market for medical devices can be fraught with obstacles. One of the first challenges confronted… Learn more
Blog articles16 June 2020 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… Learn more
Blog articles21 August 2018 4 reasons why having a single EDC system for your device company makes sense CEOs of medical device companies have an intuitive sense of what they need from their clinical data. However,… Learn more
