Statistical Methods for Design Verification, Process Validation, and Process Control 2016 is a conference that provides an introduction to the statistical tools used to analyze design verification data.
Topics
- Statistically valid sample sizes
- FDA, ISO 9001/13485, and MDD requirements
- The impact of normality and non-normality
- The significance of statistical significance
- Impact of risk analysis on choice of validation criteria
Who should Attend
Attendees with job titles such as:
- Process Engineer
- QA/QC Supervisor
- QC/QC Technician
- Manufacturing Engineer
- R&D Engineer
- Manufacturing Technician
