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Statistical Quality Control in Pharmaceutical and (IVD Industries)
Presented By Netzealous LLC DBA - Compliance4All
Wednesday, December 5th at 10:00am PST
Online sale ends: 12/04/18 at 10:00pm PST
Online
161 Mission Falls Lane, Suite 216,
Fremont, CA 94539
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Talent
Description
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 Additional Information
One Dial-in One Attendee
Price: $150.00
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Presented By
10:00am to 11:00am
General Admission: $150.00
All Ages
50 18004479407 UPCOMING EVENTS
PAST EVENTS
Monday, October 22nd
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