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…
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.
Guide to using Electronic Data Capture (EDC) for Medical Device & Diagnostics Trials
Download this guide to learn how to incorporating an Electronic Data Capture (EDC) system in your medical or diagnostics device trials.
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…
eConsent – The Enrollment Solution for Decentralized Trials
Join this webinar to understand how eConsent works, where it falls in the regulatory guidelines & see a practical demonstration of eConsent software.
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….
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.
Jumpstart Your Medical Device Preclinical Phase
The path to market for medical devices can be fraught with obstacles. One of the first challenges confronted…
6 essential steps to ensure MDR compliance before May 2021
A recent report surveying representatives from the medical device industry across the world found that more than 55%…