Medical Software Validation for the New FDA Inspections

Website https://www.compliance4all.com/webinar/medical-software-validation-for-the-new-fda-inspections-50319 | Edit Freely

Category

Deadline: July 21, 2020 | Date: July 21, 2020

Venue/Country: Online event, U.S.A

Updated: 2020-05-25 20:14:48 (GMT+9)

Call For Papers - CFP

This course will teach how to conduct a software validation program that will satisfy FDA requirements and produce a safe product.

We will explain the role of risk analysis in validation. How software requirements are used in validation will be described. This course is NOT a programming course. We will discuss what must be done but will not discuss methods to execute necessary testing.

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

Areas Covered in the Session:

Software Validation more than Testing

Requirements Traceability

Risk Analysis

Unit,Integration and System Testing

Algorithm Validation

Challenges to the Software

Configuration Management

Who Will Benefit:

Engineer

Engineer Management

Software Engineer

Programmer

Quality Assurance

Regulatory

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.

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