An Essential Guide To Eu Regulatory Affairs 2013

  • 11-12 Feb 2013
  • Harrington Hall Hotel, London, United Kingdom

Description

An Essential Guide To Eu Regulatory Affairs 2013 covers topics such as:

  • Scientific advice procedure
  • EU Regulatory Legislative Framework
  • The impact of paediatric investigational plans and how to plan for the best possible outcome
  • What areas should you focus on and what are the potential pitfalls
  • What are the timings and thresholds
  • How to manage the orphan drug designation procedure
  • The impact of the Centralised Procedure for registering medicinal products in the EU
  • The importance of the Risk Management Plan

Past Events

Important

Please, check "An Essential Guide To Eu Regulatory Affairs" official website for possible changes, before making any traveling arrangements

Event Categories

Health & Medicine: Pharma

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