Crucial for safeguarding the health of the patients and safe use of the drug, case processing becomes increasingly difficult and time-consuming, as the volume of AE reports increases exponentially. Optimisation of this work will allow your team to cope with the growing amount of work while maintaining a high quality of case processing.

Join our new free webinar “Optimising Your Case Processing: A Practical Approach” to learn how to transform your case processing making it leaner and less time-consuming while maintaining the highest quality of work. The webinar will be followed by an interactive Q&A.

Register now for the free webinar “Optimising Your Case Processing: A Practical Approach”

When?

17th of June, 4 PM CEST

How to join?

Click here to sign up

What will you learn?

  • How to identify the most time-consuming tasks with high optimisation benefit
  • How to optimise key steps of the case processing process
  • How to enhance the efficiency of your pharmacovigilance team
  • How to reduce the risk of human error in case processing

Who will be the speaker?

Stefania De Santis – Director of Pharmacovigilance, seQure

Stefania has been working in pharmacovigilance since 1985. Prior to joining seQure she held the position of Head of Corporate Drug Safety and qualified Deputy EU QPPV in a large pharmaceutical company where she managed the Pharmacovigilance Department ensuring timely and quality delivery of projects. During her career, she has been responsible for a variety of pharmacovigilance operations in both pre-registration and post-marketing settings, case processing, PSUR and DSUR preparation, ICSR/SUSAR electronic transmission to the EMA, safety database validation, safety variations, signal detection, RMPs development, SDEA/Safety Management Plans and liaising with regulatory authorities.

Stefania is a qualified EU-QPPV and certified by EMA for the use of Eudravigilance and XEVMPD.

Sign up for the free webinar “Optimising Your Case Processing: A Practical Approach”

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