This document is designed to provide concrete recommendations to all responsible stakeholders  on the general principles and best practices for medical device cybersecurity (including in vitro diagnostic (IVD) medical devices). In general, it outlines recommendations for medical device manufacturers, healthcare providers, regulators, and users to: employ a risk-based approach to the design and development of medical devices with appropriate cybersecurity protections; minimize risks that could arise from use of the device for its intended purposes; and to ensure maintenance and continuity of critical device safety and effectiveness.

Download the document :Principles and Practices for Medical Device Cybersecurity