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ven. 08 sept.

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Zoom Webinar Pharmacovigilance Global PVS

Audit and Inspection in Pharmacovigilance

In collaboration with the Global PV Society and the JPADR, Lucky Link aims to facilitate the sharing of knowledge regarding diverse approaches to PV audits and inspections across countries. This initiative seeks to improve patient safety on a global scale.

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Audit and Inspection in Pharmacovigilance
Audit and Inspection in Pharmacovigilance

Heure et lieu

08 sept. 2023, 11:00 – 13:30 UTC+2

Zoom Webinar Pharmacovigilance Global PVS

À propos de l'événement

Join us for an engaging webinar on Pharmacovigilance, organized by the Global PV Society, the journal JDAPR, and Lucky Link.

Our distinguished speakers from around the world, including India, Europe, UAE, and more, will share their expertise and perspectives on different approaches to auditing and inspections in PV. By gaining insights into these crucial topics, we aim to enhance patient safety to an even greater extent

Here's what you can expect to learn:

  1. Harmonisation of PV process: Discover the importance of aligning pharmacovigilance processes across regions and explore strategies for achieving harmonization.
  2. Improve quality ICSRs: Gain practical tips and best practices for enhancing the quality of Individual Case Safety Reports (ICSRs), ensuring accurate and comprehensive reporting.
  3. Audit and Inspection Preparedness: Learn how to effectively prepare for audits and inspections, ensuring compliance with regulatory requirements and fostering a culture of continuous improvement.
  4. Keeping an eye on regulatory updates: Stay up-to-date with the latest regulatory developments and learn how to adapt pharmacovigilance practices accordingly.
  5. Learning aspects of automation in PV: Explore the benefits and challenges of automation in pharmacovigilance and gain insights into leveraging technology for efficient and streamlined processes.
  6. Management of signals: Understand the process of signal management and learn effective approaches for detecting, evaluating, and managing safety signals.
  7. Data management: Discover strategies for efficient data collection, storage, and analysis, ensuring reliable and high-quality pharmacovigilance data.
  8. Risk-Benefit evaluation in a timely manner: Explore methodologies for timely and robust risk-benefit evaluations, enabling informed decision-making regarding the safety and efficacy of medicinal products.
  9. Good Documentation Practice: Gain an understanding of the principles and practices of good documentation in pharmacovigilance, ensuring traceability, accuracy, and compliance.

Don't miss this unique opportunity to hear from experts representing diverse perspectives from around the globe. 

Register now.

Billets

  • Pharmacovigilance Professional

    50,00 €
    + 1,25 € de frais de service
    Vente expirée
  • Others

    Quality Assurance Professionals/ Students/ Academia/ Clinical research Professionals

    10,00 €
    + 0,25 € de frais de service
    Vente expirée

Total

0,00 €

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