Clinical Research Training for Senior CRAs

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Wichtige informationen

  • Kurs
  • Fortgeschritten
  • München
  • 16 Lehrstunden
  • Dauer:
    2 Tage

To provide an update on current European regulatory requirements. To refine knowledge of ICH-GCP. To highlight important elements of the monitoring plan. To explain the elements of efficient site management. To overview safety issues. To be prepared for audits.
Gerichtet an: Site Manager, Junior CRA, CRA, Clinical Research Associate, Study Coordinator, ...

Wichtige informationen

Wo und wann

Beginn Lage
auf Anfrage
Albrechtstrasse 14, 80636, Bayern, Deutschland
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Was lernen Sie in diesem Kurs?



Gerald Van Roey
Gerald Van Roey


In this two-day course, you receive an update of the current European legislation on clinical research, you learn how to upgrade monitoring methods and skills, how to select the right investigators, how to boost recruitment of clinical trial subjects, how to solve site management issues and how to deal with non-compliance. You gain insights in monitoring plan development, tracking tools, accurate monitoring visit reporting, safety reporting and how to be prepared for audits and inspections.

This course has been specifically designed for people with at least 2 years’ experience as a Clinical Research Associate (CRA) and who want to set new goals and objectives in their career.

Erfolge des Zentrums

Zusätzliche Informationen

Preisinformation: Online or via bank transfer

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