CMPMS Trademark

Software as a service (SAAS) services featuring software for use by medical device manufacturers and regulatory professionals to manage post-market surveillance, complaint handling, adverse event tracking, signal detection, field safety corrective actions, and regulatory reporting under international compliance standards including FDA and EU medical device regulation (MDR) and in vitro diagnostic regulation (IVDR); Software as a service (SAAS) services featuring software for cloud-based applications for use by medical device manufacturers, in vitro diagnostic (IVD) companies, and regulatory consultants to manage post-market surveillance and compliance activities, and software using artificial intelligence for natural language processing for complaint classification, predictive analytics for detecting emerging medical device safety signals, and rules-based automation to support regulatory reporting workflows under international compliance standards including FDA and EU medical device regulation (MDR) and in vitro diagnostic regulation (IVDR)