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25th Annual EuroMeeting


Registration fees

The prices below are industry pricing. Reduced pricing may be available for Nonprofit/Academia and Government, subject to eligibility verification. Click Register to get pricing appropriate for your work setting. Review the cancellation and transfer policy.

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  • Tutorial 01: Highlights on the Implementation of the New Pharmacovigilance Legislation with regards to Adverse Reaction Reporting Rules, Use of New International Standards and Signal Management in Eudravigilance €380
  • Tutorial 02: Analysis of Safety Data from Clinical Trials €380
  • Tutorial 03: Update on Practical Work with Variation Regulation €380
  • Tutorial 04: Introduction to Medical Device Regulation €380
  • Tutorial 05: Recent and Current developments in Pharmaceutical Law €380
  • Tutorial 07: The Dialogue and Negotiation Process Between Applying Company and the Paediatric Committeeof the European Medicnies Agency €380
  • Tutorial 08: Health Technology Assessment of Drugs and Medical Devices €380
  • Tutorial 09: The European QP for Pharmacovigilance: Everything you ever Wanted to know but were afraid to ask €380
  • Tutorial 10: Non-Clinical Safety Assessment in Global Pharmaceutical Development €380
  • Tutorial 11: Interactions between Regulatory and Intellectual Property, Privacy and Product Liability €380
  • Tutorial 12: Development Safety Update Report (DSUR) Kick-off in 2011: Then and Know €380
  • Tutorial 13: Technology Transfer for Biopharmaceuticals Workshop €380
  • Tutorial 14: Pharmacovigilance Audits and Inspections €380
  • Tutorial 15: Coding with Confidence €380
  • Tutorial 16: Understanding Translational Medicine: Benefits and Innovative Approaches €380
  • Tutorial 17: Creating Compliant Clinical Study Reports for the EU and US €380
  • Roundtable 01: GCP Inspections and Audit Findings €200