Our GxpMedicalDevices application suite is designed specifically for the medical device sector and also for IVDs. It allows you to digitize all your critical applications to ensure 100% compliance of your products.
Our applications cover the entire life cycle of medical devices from Design, Risk Analysis, Validation and Quality Management System.
During our last webinars, we have already presented the digitization of MIR 7.2.1 and FSCAR forms. We have also covered Audit Management, and most recently Risk Analysis. In this new webinar of the GxpMedicalDevices global offer, we will summarize all these presentations in one complete session.