Test Method Validation to Verify the Performance of a Medical Device 2019 is a webinar that covers topics such as:
- Quality System Regulation, 21 CFR Part 820, and ISO 13485 - Overview
- Test Method Validation - Overview
- Qualification vs Validation
- When should Methods be Validated?
- How to perform successful test method validations
- Types of Test Method Validations
- Detailing real-life case studies
- How to ensure your inspection of verification is effective
- FDA requirements for TMV
- Understanding global reference standards for test method validation
- Recommendations: Some Best Practices and Strategies
- How to prove your inspection method is repeatable and reliable
Test Method Validation to Verify the Performance of a Medical Device 2019 is intended for:
- Document Control
- Operations Teams
- Device Development Teams
- Design Assurance Teams
