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Free seminar on ‘Pharmacovigilance considerations in drug development’

Published on: 25/09/2017

Where: Evenlode Boardroom, Milton Park Innovation Centre

When: 22 November 2017

 

Topics:

  • Early-to-late phase clinical trial pharmacovigilance
  • Preparation for Marketing Authorisation
  • Pharmacovigilance auditing and training
  • Common pharmacovigilance inspection findings and pitfalls (MHRA, BfArM)
  • Need for good, efficient processes

 

This seminar may be useful for the following:

  • - Head of Research and Development
  • - Clinical Project Managers
  • - Procurements / Contracts Management
  • - Quality Assurance

 

There will also be time available after the seminar to have a complimentary one-to-one session to discuss any company specific pharmacovigilance and regulatory affairs questions (confidentiality agreements can be signed).

 

Please register your interest by emailing: seminars@eudrac.com 

Please visit our website at www.eudrac.com

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