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Statistical Quality Control in Pharmaceutical and (IVD Industries)

 
  October 26, 2018  
     
 
Netzealous LLC DBA - Compliance4All, Online
2018-12-05


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

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
 
 
Organized by: Event Manager
Invited Speakers:
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. 
 
Deadline for Abstracts: 2018-12-04
 
Registration: https://www.compliance4all.com/control/w_product/~product_id=502227LIVE?channel=hum-molgen_Dec_2018_SEO
E-mail: support@compliance4All.com
 
 
   
 
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