Quality Management in Pharma and Biotech - Quality and safety of biopharmaceuticals: from genetics to downstream processing

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Date: 
7 Apr 2010 - 9 Apr 2010
Location: 
Varies per Module

   

This course offers an integrated approach on quality management in the pharma-ceutical, biotechnological, medical device industries and hospitals to safeguard the quality of their products. Expert knowledge and real life case studies are combined and presented and coached by professionals from Industry, Universities and Health Care Inspectorates. The training is interactive.

Module 1:
12 - 14 October 2009

Quality Management, the role of the Qualified Person

Module 2:
30 November - 3 December 2009

GxP’s applied in drug development within the pharmaceutical industry and hospital pharmacy

Module 3:
3 - 5 Februari 2010

Sterile manufacturing

Module 4:
7 - 9 April 2010

Quality and safety of biopharmaceuticals: from genetics to downstream processing


Target Audience:

  • Professionals in pharmaceutical, biotechnological and medical device industries
  • Professionals in institutions and Contract Research Organisations (CRO’s)
    Hospital pharmacists
  • Postgraduate students

 

More information, registration, and description of all modules:

http://www.bsdl-edu.bt.tudelft.nl/content/trainingcourse.html

22/01/2010