An Introduction for Pharmacovigilance Managers - Start your career in Drug Safety
Are you new to pharmacovigilance and looking to kick-start your career? Then this online course is just for you. Gain a comprehensive overview of pharmacovigilance, regulatory requirements in the EU and implementation in only two days. Book now!
- Regulatory framework and EMA GVP modules
- Management of side effects and signals
- Benefit-risk assessment and risk management
- Important pharmacovigilance documents
- Interfaces with other departments and quality management
| Veranstaltungs-Code | FB24-501396-61077534 |
Bildungsziel der Schulung:
This online course provides comprehensive knowledge on all the essentials of pharmacovigilance over two days. It equips participants with the necessary tools to confidently fulfil their responsibilities in the various aspects of pharmacovigilance.
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The course will enable you to:
- Describe the mechanisms of pharmacovigilance in Europe.
- Classify information on adverse drug reactions including MedDRA coding.
- Properly assess the responsibilities of pharmacovigilance officers.
- Understand the significance of pharmacovigilance and risk management systems.
- Comply with risk assessment procedures.
Veranstaltungsort:
Online-Webinar
weitere Orte/Termine
Kursart:
Online-Webinar
Kostenlos Info anfordern
