- TypeWebinar
- Location Baltimore, Maryland, United States
- Date 19-09-2018
Education/Teaching/Training/Development
Communications
FDA requires that all software in computer systems used in GxP activities must be validated. Validation of computer system software is completely different than validation of device software (embedded software). Validation is more than testing. It is testing plus design control and configuration management.
How to plan and conduct a risk based validation will be explained. Overall risk for computer system is a combination of software complexity and product risk as determined by probability, severity and detectability rankings. Also involved in the risk evaluation is the requirement for purchased software supplier qualification. You’ll learn how to integrate risk based supplier evaluation into the validation process.
Validation Master plan and System Validation Plans will be explained
Testing, based on risk, includes requirements validation and IQ, OQ and PQ. A procedure for each level of complexity and risk will be described.
Why ?
Validation of computer system software is completely different than validation of device software (embedded software). Attempting to conduct a CSV following device software validation concepts could result in a 483 or rejection of a product approval submission.
You will learn in detail:
Areas Covered in the Session :
Who Will Benefit:
Venue: Online Speaker Name: Edwin Waldbusser Price : $ 229 Wednesday, September 19, 2018 EST 13:00 Duration : 60 Minutes Tel: +1-844-216-5230 www.compliancetrainingpanel.com