Preparing the Marketing Authorization Application in the EU, with a focus on the product information 2018

  • 18-19 Apr 2018
  • Hilton Zurich Airport, Switzerland

Description

Topics
  • Package Leaflet
  • SmPC
  • Readability testing
  • Labelling
  • How to conduct presubmission meetings with the EMA and Rapporteurs
Who should Attend

Regulatory affairs personnel involved in development of medicinal products.

Past Events

Important

Please, check "Preparing the Marketing Authorization Application in the EU, with a focus on the product information" official website for possible changes, before making any traveling arrangements

Event Categories

Government & Global Issues: Law & Regulations
Health & Medicine: Medical device, Pharma
Technology: Biotechnology

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