Forum Institut für Management GmbH

      First Accredited Diploma in Pharmacovigilance for the Middle East - Certified by Forum · Institut für Management GmbH, Germany in cooperation with SIPS

      Forum Institut für Management GmbH
      Online

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      Wichtige informationen

      Tipologie Seminar
      Methodologie Online
      Dauer 1 Tag
      Beginn 31.12.2019
      • Seminar
      • Online
      • Dauer:
        1 Tag
      • Beginn:
        31.12.2019
      Beschreibung

      Do you need detailed information about the European Pharmacovigilance framework in order to understand and implement the
      new Common Arab Guidelines in Pharmacovigilance in your country? We would like to invite you to join our 12 live recorded
      webcasts, where European and Middle East experts will inform you of the concepts and challenges in drug safety that you need to
      remain compliant with your current PV legislation.


      Each webcast will be a two-hour webcast, delivering the information with supporting slides (also for your personal download). You can start at any time and are able to retrieve the webcasts and additional documents from our e-learning centre for six full months. An online assessment completes each webcast, giving you the possibility to receive a personal certificate after all 12 webcasts.

      Einrichtungen (1)
      Wo und wann
      Beginn Lage
      31.Dez 2019
      Online
      Beginn 31.Dez 2019
      Lage
      Online

      Zu berücksichtigen

      · An wen richtet sich dieser Kurs?

      This webcast series will be of benefit to all those working in pharmacovigilance or in related departments requiring essential drug safety expertise. Basic pharmaceutical knowledge is recommended but not a prerequisite.

      Fragen & Antworten

      Teilen Sie Ihre Fragen und andere User können Ihnen antworten

      Was lernen Sie in diesem Kurs?

      Management
      GmbH

      Themenkreis

      - Qualified person for pharmacovigilance (QPPV) - Pharmacovigilance system master file (PSMF) and PSSF - Drug adverse reactions and signal management - Risk management plan (RMP) and risk management system - Periodic safety update reports (PSUR) - Pharmacovigilance inspection and audit readiness

      Vergleichen Sie und treffen Sie die beste Wahl:
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