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2014 - Webinar On Systems Validation Made Easy

Date2014-06-12

Deadline2014-06-12

VenueMississauga, ON, Canada Canada

Keywords21 CFR Part 11 ; Systems Validation; Systems validation process

Websitehttps://compliancetrainings.com/SiteEngi...

Topics/Call fo Papers

This seminar will discuss the basics of computerized systems validation and the procedural controls to maintain compliance. Validation is on-going effort from development all the way to eventual retirement. You will hear about validation plans, user requirements, test plans, test reports, change controls, standard operating procedures, data backup and business continuity. Case studies will be used to highlight common issues and potential solutions.
Areas Covered in the Session :
Validation Plans, Requirements, Specifications, and Test Reports
Recommended SOPS
Change control
Data backup and business continuity
Tips when validating COTS software
Common audit findings and tips for a successful audit
Who Will Benefit:
This webinar is a must attend for:
Everyone involved in computer system validation
Anyone selecting computer systems intended for FDA regulated environments
Information technology professionals responsible for files or network locations
Quality professionals who organize, document and verify system compliance
Executives evaluating requirements Part 11 compliant systems
For bookings and more information contact
Compliance Trainings
5939 Candlebrook Ct,
Mississauga, ON L5V 2V5,
Canada
Customer Support : #416-915-4458
Email : support-AT-compliancetrainings.com

Last modified: 2014-04-26 21:38:01