This webinar will provide valuable assistance to all regulated companies that need to validate their systems In this session we will introduce basic control charting and statistical methods to determine if a process is capable of consistently producing product within specifications and how to make it capable if it is not
Why Should You Attend:
This is session 3 in the series of sessions for process validation using Six Sigma methods. In this session we will introduce basic control charting and statistical methods to determine if a process is capable of consistently producing product within specifications and how to make it capable if it is not. We will also learn how to measure the long term performance of a process with respect to meeting specifications.Areas Covered in the seminar:
- Xi, MR Control Charts
- Bar, R Control Charts (Xbar, s Control Charts)
- Process Capability (Cp, CpK)
- Process Performance (Pp, PpK)
Who Will Benefit:
This webinar will provide valuable assistance to all regulated companies that need to validate their systems, including companies in the Medical Device, Diagnostic, Pharmaceutical, and Biologics fields. The employees who will benefit include:- End-users responsible for processes requiring validation
- QA managers and personnel
- Validation specialists
- Consultants
- Quality system auditors
- Process Engineers
Course Provider
Lawrence Mucha,
