Computer Systems Validation | May 3, 2018 1:00 PM - May 3, 2018 2:30 PM | Automation.com

Computer Systems Validation

Event Summary

DATE:
May 3, 2018
START DATE/TIME:
May 3, 2018 1:00 PM
END DATE/TIME:
May 3, 2018 2:30 PM
TIME ZONE:
EVENT TYPE:
Webinar
HOST:
Training Doyens
PHONE:
+1-720-996-1616
EMAIL:
[email protected]
WEBSITE:
Click here to Visit

Description

OVERVIEW
This will cover the history of Computer Systems Validation in the Pharmaceutical and Medical Device industries. This led to the regulation 21 CFR Part 11, which covers the management of both electronic signatures and electronic records.
Compliance to relevant regulations using Standard Operating Procedures and required documentation will be covered.
The roles of Audits, Quality Assurance, and Risk Management will also be covered.
WHY SHOULD YOU ATTEND
Changes continue to be implemented in many existing computer systems and in many cases computer systems are being replaced or upgraded using new technologies.
Many of these changes require Validation and Validation typically involves almost everyone who uses or supports the systems.
Doing Validation is a “Project” that requires participation of many of those involved in the system. Some of this involves strong management commitment to the accuracy and quality of the products of the systems.
AREAS COVERED
• History of Validation Regulations
• Some CSV Standards to use
• Standard Operating Procedures
• Necessary Documentation
LEARNING OBJECTIVES
• Understand Computer Systems Validation
• Cover The role of Electronic Records
• Learn the Compliance to 21 CFR Part 11
• The role of Qualification in Validation
• Preparation of Standard Operating Procedures
• The Documentation needed for Validation
WHO WILL BENEFIT
• IT Staff
• Computer System Users
• Quality Assurance
• Regulatory
• System Vendors

For more detail please click on this below link:
https://bit.ly/2G8q7zu

Email: [email protected]
Toll Free: +1-888-300-8494
Tel: +1-720-996-1616
Fax: +1-888-909-1882


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