The New Clinical Trials Regulation and Regulatory Affairs Aspects of Medicinal Product Development in the EU 2017

  • 15-16 Jun 2017
  • Hilton Zurich Airport, Switzerland

Description

The New Clinical Trials Regulation and Regulatory Affairs Aspects of Medicinal Product Development in the EU 2017 covers topics such as:

  • Pricing and reimbursement issues in your development
  • Developing a regulatory strategy
  • Scientific advice and how to choose between centralised and national scientific advice
  • Orphan medicinal Products
  • Advanced Therapy Medicinal Products
  • Paediatric Investigation Plans
  • Oncology medicinal products

The New Clinical Trials Regulation and Regulatory Affairs Aspects of Medicinal Product Development in the EU 2017 brings together Regulatory Affairs personnel involved in Development of medicinal products.

Past Events

Important

Please, check "The New Clinical Trials Regulation and Regulatory Affairs Aspects of Medicinal Product Development in the EU" official website for possible changes, before making any traveling arrangements

Event Categories

Business: Innovations, Quality assurance
Health & Medicine: Healthcare, Hospitals & Clinics, Medical device, Medical laboratories, Medical technology

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