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  HUM-MOLGEN -> Events -> Meetings and Conferences  
 

To Facilitate a Closed-Loop Problem Resolution System

 
  November 23, 2017  
     
 
Netzealous LLC DBA - Compliance4All, Online
2018-01-17


Overview:
Defined Failure Investigation and Root Cause Analysis is a major tool in 

product complaint, non-conformance, and OOS failure investigations.

Why should you Attend: 
Expectations for meaningful CAPA, supported by results-driven Failure 

Investigation and Root Cause Analysis, that addresses and resolves 

underlying product problems, are growing among regulatory agencies 

world-wide.

Areas Covered in the Session:
Regulatory "Hot Buttons"
The 4 Basic Steps to Problem Solving
A Suggested Investigation Template
ID / Document the Problem - CAPA, et al

Who Will Benefit:
Senior management in Drugs, Devices, Biologics, Dietary Supplements
QA
RA
R&D
Engineering
Production
Operations


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:
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.
 
Deadline for Abstracts: 2018-01-16
 
Registration: http://www.compliance4all.com/control/w_product/~product_id=501648LIVE?channel=molgen_Jan_2018_SEO
E-mail: support@compliance4All.com
 
   
 
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