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.
Key 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
Past Events
Statistical Methods for Design Verification, Process Validation, and Process Control 2016 - 08-09 Dec 2016, Courtyard Houston Downtown /Convention Center, Texas, United States (63439)
Statistical Methods for Design Verification, Process Validation, and Process Control 2026
Important
Please, check "Statistical Methods for Design Verification, Process Validation, and Process Control" official website for possible changes, before making any traveling arrangements
Event Categories
Health & Medicine: Healthcare, Medical device, Medical laboratories, Pharma
