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

Webinar on Risk-based Outsourcing

 
  March 18, 2016  
     
 


Compliance Trainings, Online
2016-04-11


Description :

The regulatory background for the Pharmaceutical industry as a whole now requires a ‘risk based approach’ to all activities and that will of course include Outsourcing. Lack of Outsourcing Oversight is a very common finding during audits and regulatory inspections. One vital part of outsourcing is establishing adequate auditable documentation.

This course provides an understanding of risk management principles and makes the links necessary between them and the processes necessary for effective outsourcing.

Areas Covered in the Session :

Review the clinical outsourcing and the 5 steps of risk management

Outline why a 'risk-based approach' is necessary in vendor management

Review the process of vendor management and apply a risk based approach

Prioritise risks and plan mitigation actions during the vendor selection process

Examine the challenges with multiple contractors, 3rd party outsourcing and working with Academia

Who Will Benefit:

A must attend webinar for all:

Clinical Research Associates

Monitors

Data Management Team

Project Management Statisticians

Clinical Research Outsourcing

Drug Suppliers

 

All clinical research professional embarking on a risk-based approach

 
 
Organized by: Compliance Trainings
Invited Speakers:

Jane Tucker :
Over the past 28 years Jane has moved from routine data cleaning activities, via computer system validation onto training and data quality activities, eventually specializing in Quality Risk Management. Jane has worked for a variety of large pharmaceutical companies and CROs before retiring from GlaxoSmithKline. Jane now operates as a Risk Management Trainer and Consultant, specializing in Study Level Risk Management and Risk Based Monitoring as well as facilitation of risk assessment workshops.

Sue Fitzpatrick :
Sue Fitzpatrick joined the Pharmaceutical Industry in 1980. She has been responsible for the management and audit of CRAs and clinical trials in a wide range of therapeutic areas. As former Head of Education and Training at the Institute of Clinical Research she was responsible for the provision of training courses for the industry and postgraduate courses in collaboration with several UK Universities.

 
Deadline for Abstracts: 2016-04-11
 
Registration:

For more information about this event please visit

https://compliancetrainings.com/SiteEngine/ProductDetailView.aspx?id=FDB1853

 

To register this webinar

https://compliancetrainings.com/siteengine/Login.aspx 

E-mail: suzzane.d@compliancetrainings.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.