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Pharmacovigilance: ADR Management and Reporting & Outsourcing Trends, A New Drug Safety Webinar from Xtalks
Date:11/22/2013

Toronto, Canada (PRWEB) November 22, 2013

Join Dr. Marcin Marciniak, Director Drug Safety & Pharmacovigilance, PregLem SA, and member of Gedeon Richter Group and Dr. Philip Jones, BMBS, MA, MSc, PhD, Associate Director & Deputy QPPV, Symogen Limited for an in depth webinar on Adverse Drug Reaction Management and Reporting and Pharmacovigilance Outsourcing Trends.

During this webinar, the following points will be discussed:

Adverse Drug Reaction Management and Reporting

  • Key Requirements
  • Timeliness for expedited reporting
  • Reporting to EudraVigilance
  • Tools and internal industry solutions for being compliant with regulations

Pharmacovigilance Outsourcing Trends

  • Benefits and challenges involved in outsourcing pharmacovigilance processes
  • Advantages and disadvantages of outsourcing
  • Choosing a pharmacovigilance provider
  • Working with your PV provider
*Ensuring oversight of out-sourced activities
  • Brief insights into the role of pharmacovigilance throughout the product lifecycle from clinical development to patient care
  • Presenting a PSUR to external regulatory authorities
  • Main pitfalls
  • Completing the risk-benefit analysis

A live Q&A with the audience will follow the main presentation.

For more information about this online seminar or to register, go to http://xtalks.com/xto676-pharmacovigilance-ADR-outsourcing.ashx.

Xtalks, powered by Honeycomb Worldwide Inc., is a leading provider of educational webinars to the global Life Sciences community. Every year thousands of industry practitioners (from pharmaceutic
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