Professional development - Tutorials at EuroMeeting2013 4 March in Amsterdam

TUTORIAL (17)

• Title: 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
  Event Type: TUTORIAL

  Day: Monday, Mar, 04
  Time: 9:00AM - 12:30PM
• Title: Tutorial 02: Analysis of Safety Data from Clinical Trials
  Event Type: TUTORIAL
  Tracks: Theme 03 - Legal/Transparency-Risk Assessment

  Day: Monday, Mar, 04
  Time: 9:00AM - 12:30PM
• Title: Tutorial 03: Update on Practical Work with Variation Regulation
  Event Type: TUTORIAL
  Tracks: Theme 03 - Legal/Transparency-Risk Assessment

  Day: Monday, Mar, 04
  Time: 9:00AM - 12:30PM
• Title: Tutorial 04: Introduction to Medical Device Regulation
  Event Type: TUTORIAL
  Tracks: Theme 03 - Legal/Transparency-Risk Assessment

  Day: Monday, Mar, 04
  Time: 9:00AM - 12:30PM
• Title: Tutorial 05: Recent and Current developments in Pharmaceutical Law
  Event Type: TUTORIAL
  Tracks: Theme 03 - Legal/Transparency-Risk Assessment

  Day: Monday, Mar, 04
  Time: 9:00AM - 12:30PM
• Title: Tutorial 7: THE DIALOGUE AND NEGOTIATION PROCESS BETWEEN APPLYING COMPANY AND THE PAEDIATRIC COMMITTEE OF THE EUROPEAN MEDICINES AGENCY 
  Event Type: TUTORIAL
  Tracks: Theme 03 - Legal/Transparency-Risk Assessment

  Day: Monday, Mar, 04
  Time: 9:00AM - 12:30PM
• Title: Tutorial 08: Health Technology Assessment of Drugs and Medical Devices
  Event Type: TUTORIAL
  Tracks: Theme 03 - Legal/Transparency-Risk Assessment

  Day: Monday, Mar, 04
  Time: 9:00AM - 12:30PM
• Title: Tutorial 09: The European QP for Pharmacovigilance: Everything you ever Wanted to know but were afraid to ask
  Event Type: TUTORIAL
  Tracks: Theme 03 - Legal/Transparency-Risk Assessment

  Day: Monday, Mar, 04
  Time: 9:00AM - 12:30PM
• Title: Tutorial 10: Non-Clinical Safety Assessment in Global Pharmaceutical Development 
  Event Type: TUTORIAL
  Tracks: Theme 03 - Legal/Transparency-Risk Assessment

  Day: Monday, Mar, 04
  Time: 9:00AM - 12:30PM
• Title: Tutorial 11: Interactions between Regulatory and Intellectual Property, Privacy and Product Liability
  Event Type: TUTORIAL
  Tracks: Theme 03 - Legal/Transparency-Risk Assessment

  Day: Monday, Mar, 04
  Time: 9:00AM - 12:30PM
• Title: Tutorial 12: Development Safety Update Report (DSUR) Kick-off in 2011: Then and Know
  Event Type: TUTORIAL
  Tracks: Theme 03 - Legal/Transparency-Risk Assessment

  Day: Monday, Mar, 04
  Time: 9:00AM - 12:30PM
• Title: Tutorial 13: Technology Transfer for Biopharmaceuticals Workshop
  Event Type: TUTORIAL
  Tracks: Theme 03 - Legal/Transparency-Risk Assessment

  Day: Monday, Mar, 04
  Time: 9:00AM - 12:30PM
• Title: Tutorial 14: Pharmacovigilance Audits and Inspections
  Event Type: TUTORIAL
  Tracks: Theme 03 - Legal/Transparency-Risk Assessment

  Day: Monday, Mar, 04
  Time: 9:00AM - 12:30PM
• Title: Tutorial 15: Coding with Confidence
  Event Type: TUTORIAL
  Tracks: Theme 03 - Legal/Transparency-Risk Assessment

  Day: Monday, Mar, 04
  Time: 9:00AM - 12:30PM
• Title: Tutorial 16: Understanding Translational Medicine: Benefits and Innovative Approaches 
  Event Type: TUTORIAL
  Tracks: Theme 03 - Legal/Transparency-Risk Assessment

  Day: Monday, Mar, 04
  Time: 9:00AM - 12:30PM
• Title: Tutorial 17: Creating Compliant Clinical Study Reports for the EU and US
  Event Type: TUTORIAL
  Tracks: Theme 03 - Legal/Transparency-Risk Assessment

  Day: Monday, Mar, 04
  Time: 9:00AM - 12:30PM
• Title: Roundtable 01: GCP Inspections and Audit Findings
  Event Type: TUTORIAL

  Day: Monday, Mar, 04
  Time: 9:00AM - 12:30PM