ResearchBib Share Your Research, Maximize Your Social Impacts
Sign for Notice Everyday Sign up >> Login

2018 - Computer System Validation 2018 Fundamentals

Date2018-10-23

Deadline2018-10-22

VenueFremont, USA - United States USA - United States

KeywordsProduction Managers; Engineering Managers; Lab Managers

Websitehttps://www.compliance4all.com/control/w...t_2018_SEO

Topics/Call fo Papers

Overview:
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.
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 in the Session:
Validation strategy
Requirements documentation
Complexity and risk analysis
Creating a detailed test plan based on risk
Supplier qualification
IQ, OQ and PQ
Who Will Benefit:
Computer System Developers
Systems Development Engineers
QA/ QC
Lab Managers and Analysts
Production Managers
Engineering Managers
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.
Event Fee: One Dial-in One Attendee Price: US$150.00
Contact Detail:
Compliance4All DBA NetZealous,
Phone: +1-800-447-9407
Email: support-AT-compliance4All.com

Last modified: 2018-08-10 14:38:22