How to Prepare for PhV Audits and Inspections 2016

  • 19-20 Apr 2016
  • Mercure Paris La Défense Grande Arche, Nanterre, France

Description

How to Prepare for PhV Audits and Inspections 2016 covers topics such as:

  • Prepare responses to audit/inspection findings, including responses and corrective/preventive action (CAPA) plans
  • How to handle the actual audit/inspection and responses to requests and findings based on the:
    • The legal basis of inspections or
    • Audit/inspection methodology
    • The contractual basis of audits
  • Assess regional differences with respect to European and US FDA inspections
  • Prepare their function for an audit/inspection: roadmap, teams, tasks, and documents

How to Prepare for PhV Audits and Inspections 2016 brings together:

  • Regulatory Affairs
  • Pharmacovigilance/Drug safety (QPPV)
  • Medical Information
  • Quality & Compliance
  • Compliance
  • Risk Management
  • Management Staff Responsible for Running Inspections
  • Pharmacovigilance Auditors
  • Employees (directly and indirectly) Involved in Inspections

Past Events

Important

Please, check "How to Prepare for PhV Audits and Inspections" official website for possible changes, before making any traveling arrangements

Event Categories

Health & Medicine: Pharma

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