Search   |     Toll free: +1-800-447-9407   |

Medical Device Software Validation Meeting FDA Regulations

Instructor Edwin Waldbusser
Webinar ID 36724
22 Days Left To REGISTER

Date Tuesday, October 17, 2023
Time 9:00 AM PDT | 12:00 PM EDT
Duration 60 Minutes  

Webinar Price Details


We will explain the role of risk analysis in validation. How software requirements are used in validation will be described.

Why should you Attend

Testing software to prove that it works and has no bugs is not sufficient to obtain FDA approval. There are additional analyses and tests that FDA feels are necessary to prevent user injuries. These requirements were developed after an analysis by the FDA of many recalled medical devices. In this webinar, you will learn the testing that is required in addition to functional tests to produce a validated software product.

Handouts are software traceability matrix form, validation plan template, and validation report form.

Areas Covered in the Session

  • Software validation is more than testing
  • Requirements traceability
  • Risk analysis
  • Unit, integration, and system testing
  • Algorithm validation
  • Challenges to the Software
  • Configuration Management

Learning Objectives:

  • How to validate medical device software in compliance with FDA objectives

Who Will Benefit

  • Engineering Personnel
  • Software Developers
  • QA
  • Management

Speaker Profile

Edwin Waldbusser is a consultant retired from industry after 20 years in management of development of medical devices (5 patents). He has been consulting in the US and internationally in the areas of design control, risk analysis and software validation for the past 8 years. Mr. Waldbusser has a BS in Mechanical Engineering and an MBA. He is a Lloyds of London certified ISO 9000 Lead Auditor and a member of the Thomson Reuters Expert Witness network.