21 CFR Part 11 Compliance; specifics needed to eliminate 483s 2011
28 Feb 2011
Webinar
This 21 CFR Part 11 compliance training will guide you through the concept of part 11 and explanation of its 3 primary areas SOPs, Product features and Validation (10 step risk based approach).This is the first webinar in a series and it takes the mystery out of what is needed for 21 CFR Part 11 compliance. It will help you to eliminate 483s and Warning Letters.
Areas Covered in the Seminar:
Which data and systems are subject to Part 11.
What Part 11 means to you, not just what it says in the regulation.
Avoid 483 and Warning Letters.
Explore the three primary areas of Part 11 compliance: SOPs, software product features, and validation documentation.
Ensure data integrity, security, and protect intellectual property.
Understand the current computer system industry standards for security, data transfer, and audit trails.
Electronic signatures, digital pens, and biometric signatures.
SOPs required for the IT infrastructure.
Product features to look for when purchasing COTS software.
Reduce validation resources by using easy to understand fill-in-the-blank validation documents.
Who Will Benefit:
Computer System users
IT
QA
Managers
Executives
Past Events
21 CFR Part 11 Compliance; specifics needed to eliminate 483s 2011 - 28 Feb 2011, Webinar (12720)
21 CFR Part 11 Compliance; specifics needed to eliminate 483s 2026
Important
Please, check "21 CFR Part 11 Compliance; specifics needed to eliminate 483s" official website for possible changes, before making any traveling arrangements
