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Registration fees

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Non-Member Price

€2000

Member price:

€1885

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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

Mar 04, 2013 – Mar 04, 2013

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Tutorial 02: Analysis of Safety Data from Clinical Trials

Mar 04, 2013 – Mar 04, 2013

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Tutorial 03: Update on Practical Work with Variation Regulation

Mar 04, 2013 – Mar 04, 2013

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Tutorial 04: Introduction to Medical Device Regulation

Mar 04, 2013 – Mar 04, 2013

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Tutorial 05: Recent and Current developments in Pharmaceutical Law

Mar 04, 2013 – Mar 04, 2013

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Tutorial 07: The Dialogue and Negotiation Process Between Applying Company and the Paediatric Committeeof the European Medicnies Agency

Mar 04, 2013 – Mar 04, 2013

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Tutorial 08: Health Technology Assessment of Drugs and Medical Devices

Mar 04, 2013 – Mar 04, 2013

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Tutorial 09: The European QP for Pharmacovigilance: Everything you ever Wanted to know but were afraid to ask

Mar 04, 2013 – Mar 04, 2013

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Tutorial 10: Non-Clinical Safety Assessment in Global Pharmaceutical Development

Mar 04, 2013 – Mar 04, 2013

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Tutorial 11: Interactions between Regulatory and Intellectual Property, Privacy and Product Liability

Mar 04, 2013 – Mar 04, 2013

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Tutorial 12: Development Safety Update Report (DSUR) Kick-off in 2011: Then and Know

Mar 04, 2013 – Mar 04, 2013

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Tutorial 13: Technology Transfer for Biopharmaceuticals Workshop

Mar 04, 2013 – Mar 04, 2013

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Tutorial 14: Pharmacovigilance Audits and Inspections

Mar 04, 2013 – Mar 04, 2013

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Tutorial 15: Coding with Confidence

Mar 04, 2013 – Mar 04, 2013

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Tutorial 16: Understanding Translational Medicine: Benefits and Innovative Approaches

Mar 04, 2013 – Mar 04, 2013

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Tutorial 17: Creating Compliant Clinical Study Reports for the EU and US

Mar 04, 2013 – Mar 04, 2013

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Roundtable 01: GCP Inspections and Audit Findings

Mar 04, 2013 – Mar 04, 2013

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