Hot Spots in an Internal Audit

October 19, 2015

CfPA-The Center for Professional Advancement, 90 Minute Accredited Online Training
December 3, 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 the audit process including Auditors, Audit managers, Production supervisors and managers, Technical support such as Validation and Engineering, Quality System managers and Quality Control personnel.

Course Description

This 90 minute, accredited webinar, drawn from 40 plus years of the presenter’s experiences will discuss the areas that have been overlooked, are quick and easy to check on, that are compliance failures yielding 483 observations and even Warning Letters. This webinar will instruct simple ways to cover these 12 ‘HOT SPOTS” in order to take corrective action before they grow into major problems. These 12 areas should be an integral part of any audit system.

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 4, 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 nearly 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.

Marshall has 40 plus years of experience in cGMPs and recently has been involved with several compounders and their FDA interface.

Deadline for Abstracts:

n/a

Registration:

Please click here for registration information.

E-mail:

sberg@cfpa.com

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