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Event Details


Pharmacokinetics in Drug Development - an integrated approach

For the Non-Specialist

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Who should attend?

The course is intended for all professionals in the drug development arena especially those that work in or with clinical project teams (eg Regulatory Affairs specialists; Medical personnel; Project Managers/Leaders; Clinical Research Associates; Medical Writers) who want to further their knowledge of the usefulness of PK in their projects.


The aim of this course is to provide participants with an overview of the principles of PK and PK/PD modelling and how, together with regulatory guidances, they can be used to effectively deliver drug development programmes.

What will participants gain?

  • Increased confidence to discuss PK issues within their drug projects
  • Understanding of the common PK terms and their importance
  • Understanding of how PK data influences the clinical development Programme
  • An understanding of the factors that contribute to variability in PK
  • The role of PK/PD modelling in drug development
  • An appreciation of how regulatory guidances influence PK


Early-bird rate available until 18 May 2018


Judith Callanan

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