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Tutorial 10: Non-Clinical Safety Assessment in Global Pharmaceutical Development

Mar 4 2013 9:00AM - Mar 4 2013 12:30PM | RAI Center Europaplein 1078 GZ Amsterdam Netherlands

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Overview 

This tutorial has been prepared to provide attendees with an overview on the importance of non-clinical studies and where they fit in the pharmaceutical development.

Who Should Attend 

Non specialist in toxicology, regulatory affairs personnel, clinical colleagues, project team leaders and members

 

Learning Objectives 

At the conclusion of this tutorial, attendees will be able to:

  • Recognise objectives and strategies in toxicology of drug development
  • Describe improved use of non clinical data
  • Describe the requirements for safety by agencies

 

Instructor(s) 

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