2018 - 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 Labs
Translational research
Diagnostic Labs
Lab CRO
CMC
Quality 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: +1-800-447-9407
Email: support-AT-compliance4All.com