How can companies allocate scarce resources

MessageThis Webinar is over
Date Jun 27, 2018
Time 10:00 AM to 11:00 AM
Cost $ 150.00
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. 

And for most companies, the fixes are not rocket-science, but 

proper up-front risk-based, closed-loop failure investigation / root 

cause analysis as an integral part of CAPA, Validation and Quality 

Management Systems / cGMP planning, implementation and 


Areas Covered in the Session:
Regulatory "Hot Buttons"
The 4 Basic Steps to Problem Solving
A Suggested Investigation Template
Monitor for Effectiveness
Lock In the Change - Close the Loop
Take It to the Next Level

Who Will Benefit:
Consultants,Others Tasked with Product

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. In addition, he has successfully designed, written and 

run all types of process, equipment and software 

qualifications/validations, which have passed FDA audit or 

submission scrutiny, and described in peer-reviewed technical 

articles, and workshops, world wide.

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

Contact Detail:
Compliance4All DBA NetZealous,
Phone: +1-800-447-9407


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