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EU Health Authorities Scientific and Regulatory Advice




Nanterre, France


15 Jun 2018

Reference No: D1802236 - DIA

Apply for this event

Key points about this Training Event

  • Focus
  • Flexibility
  • Convenience
  • Cost Effectiveness
Event Description

Course Outline:

The course is built up as a dialogue between industry and regulator perspective and will teach you what authorities pay attention to, what inquiries they make and what they expect to hear from sponsors.  The focus is on authority meetings in the EU but will also touch upon FDA meeting specificities

At the conclusion of this course, participants will be able to:

  • Work with their project teams to make the right decisions regarding HA meetings
  • Present their case, make their point and use their time managing HA meetings efficiently
  • Understand how HAs think and act – by putting themselves in the shoes of the authority
  • Know how to listen to regulators, anticipate their questions
  • Implement the advice received

When & Where?

15 June 2018

Mercure Paris La Défense Grande Arche 17/20 Esplanade Ch. de Gaulle - Rue des Trois Fontanot
92000 Nanterre (Paris region)


Course fee for members of DIA: €800
Course fee for delegates : €955

Group Discount available
Register 3 individuals from the same company and receive a 50% discount for a 4th

Applicant Requirements
  • Professionals in regulatory affairs, project management and product development
Reference No: D1802236 - DIA
DIA, a non-profit association, is the only global organization dedicated to bringing health care product development professionals together in a trusted, global, neutral environment to share insights and drive action in health care product development and life cycle management


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