Statistical Quality Control in Pharmaceutical and (IVD Industries)

Overview:Process validation is the establishment of documented evidence which provides a high degree of assurance that a specific process will consistently produce a product meeting its pre- determined specifications and quality characteristics.
Areas Covered in the Session:The first step in establishing the control chart is to set the QC limits. The formula "Mean +/- 3*SD" is often taken for granted, the webinar will explain how the QC limits should be established. Why Mean?Why 3?Why SD?Why are the upper and lower limits symmetric around the mean?What N should be required to do this calculation?
Who Will Benefit:Clinical LabsTranslational researchDiagnostic LabsLab CROCMCQuality Control
Speaker Profile:Dr. Shuguang Huang has 20 years of experience working in pharmaceutical and diagnostic companies. He had assumed technical and management positions at Eli Lilly, Wyeth, Pfizer, and Precision Therapeutics, a cancer diagnostic company. In 2014, he co-founded and assumed the Chief Scientific Officer position for the statistics consulting company Stat4ward LLC.
Event Fee: One Dial-in One Attendee Price: US$150.00
Contact Detail:Compliance4All DBA NetZealous,Phone: +1-800-447-9407Email: compliance4all14@gmail.com