2019 - Scrutinizing Test Method Validation (TMV) to Verify the Performance of a Medical Device
Date2019-05-02
Deadline2019-05-02
VenueOnline Event, USA - United States
KeywordsTest method validation; 21 CFR Part 820; Quality System Regulation
Topics/Call fo Papers
Test Method Validation - Overview
Quality System Regulation, 21 CFR Part 820, and ISO 13485 - Overview
When should Methods be Validated?
Qualification vs Validation
Types of Test Method Validations
How to perform successful test method validations
How to ensure your inspection of verification is effective
Detailing real-life case studies
Understanding global reference standards for test method validation
FDA requirements for TMV
How to prove your inspection method is repeatable and reliable
Recommendations: Some Best Practices and Strategies
Quality System Regulation, 21 CFR Part 820, and ISO 13485 - Overview
When should Methods be Validated?
Qualification vs Validation
Types of Test Method Validations
How to perform successful test method validations
How to ensure your inspection of verification is effective
Detailing real-life case studies
Understanding global reference standards for test method validation
FDA requirements for TMV
How to prove your inspection method is repeatable and reliable
Recommendations: Some Best Practices and Strategies
Other CFPs
Last modified: 2019-04-07 22:32:04