When: |
03 May through 03 May 2018 | |
Where: |
Online Event | United States | |
Website URL: |
https://bit.ly/2JFvO9l | |
Sponsoring organization: |
Training Doyens | |
Categories: |
Medicine & Health - Pharmaceutical / Medicinal |
Keywords:
Event 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 ...
Read more
Posting date:
12 April 2018 | 134 views
Placement:
Not-featured (How do I make my event featured?)
Flag (Report this event)