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  4. Introduction to ISO 14971: Risk Management of Medical Device Software

Introduction to ISO 14971: Risk Management of Medical Device Software

Introduction to ISO 14971: Risk Management of Medical Device Software: Learn ISO 14971 principles for effectively managing risks in medical device software development and compliance.

Course Overview

Overall Proficiency Level
2 - Intermediate
Course Catalog Number
T101
Course Prerequisites

None

Training Purpose
Functional Development
Management Development
Specific Audience
All
Delivery Method
Online, Self-Paced
  • Online, Self-Paced

Learning Objectives

  • Understand the ISO 14971 standard for risk management.
  • Learn to apply risk management to medical device software.
  • Develop skills to identify and assess software risks.
  • Ensure compliance with ISO 14971 regulatory requirements.
  • Enhance patient safety and software reliability.

Framework Connections

The materials within this course focus on the NICE Framework Task, Knowledge, and Skill statements identified within the indicated NICE Framework component(s):

Feedback

If you would like to provide feedback on this course, please e-mail the NICCS team at NICCS@mail.cisa.dhs.gov. Please keep in mind that NICCS does not own this course or accept payment for course entry. If you have questions related to the details of this course, such as cost, prerequisites, how to register, etc., please contact the course training provider directly. You can find course training provider contact information by following the link that says “Visit course page for more information...” on this page.

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