- TypeWebinar
- Location Aurora, Colorado, United States
- Date 03-05-2018
Education/Teaching/Training/Development
Medical/Healthcare/Hospital
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
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 basics of computer system validation in pharmaceutical and medical device industries and how to stay in compliance with different regulations.