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Finding the Root Cause

 
  October 20, 2015  
     
 
CfPA-The Center for Professional Advancement, 90 Minute Accredited Online Training
December 15, 2015 at 11:00 a.m.–12:30 p.m. (ET)


Who Should Attend?
This online training will benefit professionals in the life-science industries. It is intended for any personnel involved in finding and correcting the cause of compliance issues including Auditors, Audit managers, Production supervisors and Managers, Technical support such as Validation and Engineering, Quality System managers and Quality Control personnel.

Course Description
In the follow up to a compliance problem, companies frequently fail to discover the actual root cause or combination of causes that need to be corrected. As a result, failures will repeat over and over, often because the root cause is incorrectly deemed to be simply “Lack of Operator Training.”

This 90-minute accredited training will give keys to solving this issue. It will include several case studies showing how to get to the actual root cause of the problem so that effective corrective action can be taken.

Can't Make this LIVE Webinar? 
Simply select the On Demand option when registering and we will send you the link to view the recorded version.

This course will be available On Demand: December 16, 2015
 
 
Organized by: CfPA-The Center for Professional Advancement
Invited Speakers:
William G. Marshall; President, William G. Marshall & Associates

William G. Marshall is President of William G. Marshall and Associates. He has over forty years experience in the Pharmaceutical and Medical Device Manufacturing Environment. Mr. Marshall has held Director level and Chief Operating Officer positions with large multinational pharmaceutical corporations as well as start-up ventures. He has been the Director of a major reference laboratory, and has been active in clean room design and validation. In the last five years, he has acted as a third party in several consent decrees.

Mr. Marshall is currently a consultant to the worldwide drug and device industry as well as to the FDA. He lectures worldwide in GMP related issues including Clean Room Technology and Sterilization.
 
Deadline for Abstracts: n/a
 
Registration: Please click here for registration information.
E-mail: sberg@cfpa.com
 
   
 
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