Statistical Quality Control in Pharmaceutical and (IVD Industries)

Website https://www.compliance4all.com/control/w_product/~product_id=502227LIVE?channel=ourglocal_Dec_2018_S | Edit Freely

Category Clinical Labs, Translational research, Diagnostic Labs

Deadline: December 03, 2018 | Date: December 05, 2018

Venue/Country: Online, U.S.A

Updated: 2018-10-08 14:39:33 (GMT+9)

Call For Papers - CFP

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: supportcompliance4All.com