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Corporate Recorded: Access recorded version, Any number of participants unlimited viewing for 6 months ( Access information will be emailed 24 hours after the completion of live webinar)
This course will teach how to conduct a software validation program for medical devices containing software 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.
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:
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