- TypeWebinar
- Location Aurora, Colorado, United States
- Date 06-11-2018
Education/Teaching/Training/Development
Business Development
Information Technology
Computer/Technology
Medical/Healthcare/Hospital
OVERVIEW
According to the FDA requirements 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). Computer system 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. In this computer system validation training you’ll learn how to integrate risk based supplier evaluation into the computer system 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 SHOULD YOU ATTEND
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.
AREAS COVERED
LEARNING OBJECTIVES
WHO WILL BENEFIT
For more detail please click on this below link:
Email: [email protected]
Toll Free: +1-888-300-8494
Tel: +1-720-996-1616
Fax: +1-888-909-1882
Understand the process of computer system validation in pharmaceutical industry and the FDA requirements for the same. The webinar also discusses how to integrate risk based supplier evaluation into the validation process.