Drug Safety and Pharmacovigilance September 2011

Course Description

This web seminar will deliver an introduction to the basics of drug safety and pharmacovigilance, including regulatory requirements, Adverse Event reporting, signaling, and risk management. Successful navigation of drug safety and pharmacovigilance are keys to product longevity, consumer confidence, and regulatory compliance. This web seminar will also provide learners with the regulatory references, processes, best practices, and analysis and investigation techniques to minimize risk, avoid product recall, and meet international safety and reporting standards.


Learning Objectives

  • Work to international standards by meeting regulatory requirements for product safety
  • Collect, assess, report, and analyze Adverse Events
  • Identify differences between U.S. and European legal requirements

Who Should Attend

  • Clinical Safety/Pharmacovigilance Specialists
  • Regulatory Affairs Professionals
  • Quality Management Specialists


Steve Jolley

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Course Length Time

1.5 hours; 1:00 - 2:30 p.m. Eastern

Course Dates

September 8, 2011                                

Hold this course at your company!
For more information, contact Naila Ganatra at (215) 413-2471