USFDA & EU Essentials of Drug Safety and Pharmacovigilance 2012

  • 05-07 Mar 2012
  • Mumbai, India

Description

USFDA & EU Essentials of Drug Safety and Pharmacovigilance 2012 is a seminar that covers topics such as:

  • Assessing Adverse Event Cases
  • Overview of Pharmacovigilance
  • Global Regulatory Requirements
  • Reporting Adverse Events
  • Pharmacovigilance Best Practices
  • Inspections and Audits
  • Case Studies with Real-Life Inspection Findings
  • Preparing for an Inspection
  • Pharmacovigilance and Risk Management Process
  • Background to Signal Detection
  • Signalling and Data Mining Exercises

USFDA & EU Essentials of Drug Safety and Pharmacovigilance 2012 brings together Regulatory Affairs, Pharmacoepidemiology , Pharmacovigilance Specialists, Clinical Safety Staff, Quality Management Specialists, Regulatory Affairs Professionals, Regulatory Affairs, Drug Safety and Pharmacovigilance, Executives with any Legal Responsibility for Drug Safety and Clinical Development.

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Important

Please, check "USFDA & EU Essentials of Drug Safety and Pharmacovigilance" official website for possible changes, before making any traveling arrangements

Event Categories

Health & Medicine: Healthcare, Medical device, Pharma

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