Statistical Quality Control in Pharmaceutical and (IVD Industries)

MessageThis Webinar is over
Date Dec 5, 2018
Time 10:00 AM to 11:00 AM
Cost $ 150.00
Online
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@compliance4All.com

 


comments powered by Disqus
Create your own event
Turn your passion into a business.
Join our mailing list