Online Education & Training

Click on the topics below to explore and purchase recorded webinars below. Clicking the link will take you to the Compliance Online website.

• Failure Modes and Effects Analysis (FMEA) – An Effective Tool for Risk Management
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• Design Controls Basics – From Design Inputs to Design Outputs and Effective Design Transfer
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• Design for Six Sigma in Medical Devices: Integration with the FDA Quality Systems Regulations
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• Designing in Quality via Statistical Process Control
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• Critical Parameters and Design, Process and Purchasing Controls
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• Successful Implementation Strategies of Design for Six Sigma
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• Practical Process Validations – Pack of Two Courses
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• Test Method Validation Basics – Ensuring Adequacy and Reliability of Your Test Methods
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• Gage R & R – Improving the Reliability and Reducing the Variation of Your Measurement System
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• Practical Process Validation Part 1 – Validation Planning, Prerequisites and Best Practices
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• Practical Process Validation Part 2 – Qualification Steps, Process Controls and Sustainability Strategies
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• The FDA’s New Emphasis on Supplier Controls? Is Your Company Ready?
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• What are DHF, DMR and DHR? – The FDA Quality Systems Regulations Records Explained
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