What exactly is required for 21 CFR Part 11 compliance?
08 Oct 2010
Online Event
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).
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
Past Events
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What exactly is required for 21 CFR Part 11 compliance? 2026
Important
Please, check "What exactly is required for 21 CFR Part 11 compliance?" official website for possible changes, before making any traveling arrangements
Event Categories
Business: Quality assurance
Health & Medicine: Medical device, Medical laboratories, Pharma
