TEAM-NB DOCUMENTS Code-of-Conduct-Team-NB-V5-1-20250625 25/06/2026| team-nb
Secure your code and third-party libraries with agentless runtime protection for IoT, powered by our patented technology.| Sternum IoT
Unpacking the strict medical device regulation manufacturers face, ensuring safety and efficacy as a response to the growing cybersecurity challenges impacting patient safety.| Sternum IoT
Security by design is the practice of developing software and hardware to prevent security vulnerabilities and mitigate security risks.| Sternum IoT
IEC 62443 is a set of cybersecurity standards for industrial automation and control systems (IACS), impacting manufacturers, operators and service providers.| Sternum IoT
2023 update on FDA cybersecurity guidelines for medical devices includes risk assessment, interoperability, and premarket submission details.| Sternum IoT
FBI PIN (Private Industry Notification) calls for integrity verification protection for IoMT.| Sternum IoT
Sternum enables continuous monitoring by utilizing device and fleet-level insights so you can build better products faster, resolve issues with ease, deploy at scale, and innovate with confidence.| Sternum IoT
This page provides a range of documents to assist stakeholders in applying Regulation (EU) 2017/745 on medical devices (MDR) and Regulation (EU) 2017…| Public Health
The Manufacturer and User Facility Device Experience (MAUDE) database is a searchable database of medical device reports (MDRs) of adverse events involving medical devices over the last ten years. Reports older than ten years are provided on the FDA's MDR Data Files webpage. | www.accessdata.fda.gov