home   genetic news   bioinformatics   biotechnology   literature   journals   ethics   positions   events   sitemap
 
  HUM-MOLGEN -> Events -> Meetings and Conferences  
 

Project Management for Auditors – Improving audit productivity for GCP, GMP and GLP

 
  June 20, 2012  
     
 
ComplianceOnline, Online Event
2012-07-17


Why Should You Attend:

Auditing is essential to ensuring quality assurance of drug development. Each audit has a degree of complexity which needs effective project management. With ever increasing pressures to complete the audit promptly and to the appropriate quality standard, the effective use of project management can provide essential tools and techniques to achieve this. Indeed effective project management can be a key factor to successful completion of efficient auditing.

This presentation will provide you with an excellent understanding of project management skills, to apply to auditing in all GXP areas. You will be provided with an integrated project tool kit which can easily be used with your existing or future project management tools used for auditing. This tool kit has been used to significantly improve the successful completion of auditing on time to the right quality standard in many pharmaceutical organisations.  The presentation will show you how to use these project management skills to gain the most benefit from them in your auditing activities.

 Areas Covered in the Seminar:

  • What is a Project Management framework for auditing?
  • What are the benefits and relevance of project management to  audit?
  • Key principles of project management applied to auditing
  • key project management definitions relevant to audit
  • Defining project scope and requirements for an audit project
  • Developing the Project Work Plan for an audit
  • Defining activity dependencies and creating network diagrams for an audit
  • Producing a project plan for an audit
  • Monitoring and controlling audit projects
  • Closing the audit project

 

 
 
Organized by: ComplianceOnline
Invited Speakers: Dr. Laura Brown, PhD, MBA, Diploma Clinical Sciences is an independent QA and Training Consultant in the Pharmaceutical Industry, and Course Director for the MSc in Clinical Research, School of Pharmacy at the University of Cardiff. Laura has more than 17 years experience of running clinical trials and clinical quality assurance in the pharmaceutical industry.
 
Deadline for Abstracts: 2012-07-17
 
Registration:

For Registration:

http://www.complianceonline.com/ecommerce/control/trainingFocus/~product_id=701982?channel=hummolgen 

E-mail: referral@complianceonline.com
 
   
 
home   genetic news   bioinformatics   biotechnology   literature   journals   ethics   positions   events   sitemap
 
 
 

Generated by meetings and positions 5.0 by Kai Garlipp
WWW: Kai Garlipp, Frank S. Zollmann.
7.0 © 1995- HUM-MOLGEN. All rights reserved. Liability, Copyright and Imprint.