Investigation and Root Cause Analysis to Meet FDA Expectations

Date Aug 6, 2019
Time 10:00 AM to 11:00 AM
Cost 150.00
Online
Overview:
This webinar will help you understand the critical ingredients for conducting 

an effective root cause analysis, also you will learn how to Analyze and 

document the root cause of the problem.

Why should you Attend:
The billions of dollars spent by industry annually on quality / GMP are not 

providing the product safety or efficacy seemingly promised.

Areas Covered in the Session:
Use the 7 Tools to Find the Solution(s)
Monitor for Effectiveness
Lock In the Change - Close the Loop
Take It to the Next Level

Who Will Benefit:
R&D
Engineering
Production
Operations

Speaker Profile:
John E. Lincoln is a medical device and regulatory affairs consultant. He has 

helped companies to implement or modify their GMP systems and 

procedures, product risk management, U.S. FDA responses.

Event Fee: One Dial-in One Attendee Price: US $150.00

Contact Detail:
Compliance4All DBA NetZealous,
Phone: +1-800-447-9407
Email: compliance4all14@gmail.com

 


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