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21 CFR Part 11 compliance for software validation and SaaS/Cloud
Oct 12, 2017 - 08:30 AM - Oct 13, 05:00 PM
Link to Website
Hilton Zurich Airport Hohenbühlstrasse 10, 8152 Opfikon, Switzerland,
Phone: 1 929 900 1853
Day 1 Schedule
Introduction to the FDA
How the regulations help your company to be successful
Which data and systems are subject to Part 11
21 CFR Part 11/Annex 11 - Compliance for Electronic Records and Signatures
What Part 11 means to you, not just what it says in the regulations
Avoid 483 and Warning Letters
Explore the three primary areas of Part 11 compliance: SOPs, software product features, and validation documentation
How SaaS/cloud computing changes qualification and validation
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
The Five Keys to COTS Computer System Validation
The Who, What, Where, When, and Why of CSV
Day 2 Schedule
Ten-Step Process for COTS Risk-Based Computer System Validation
Learn which documents the FDA expects to audit.
How to use the risk-based validation approach to lower costs.
How to link requirements, specifications, risk management, and testing.
Document a computer system validation project using easy to understand fill-in-the-blank templates.
Based on: "Risk-Based Software Validation - Ten Easy Steps" (Davis Horwood International and PDA - www.pda.org, 2006).
How to Write Requirements and Specifications
Workshop for writing requirements and then expanding them for specifications
How to Conduct a Hazard Analysis/Risk Assessment-Exercise
Step-by-step instructions for performing and documenting a risk assessment, and how to use the results to reduce validation documentation.
Reduce testing by writing test cases that trace to elements of risk management.
How to write efficient test cases
System Change Control
How to manage a validated system with minimal documentation
Purchasing COTS Software
How to purchase COTS software and evaluate software vendors.
Cost Reduction Without Increasing Regulatory or Business Risk
How to save money
How to increase quality
How to increase compliance with less documentation
FDA Compliance Specialist,
BUSINESS & MANAGEMENT CONFERENCES,
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