Regulatory Lifecycle Management - Maintenance and sustainment of human medicinal product approvals
This course familiarises you with regulatory post-approval duties and provides first-hand information on variation submission, PV activities and labelling changes.
- Time and deadline management in the
product lifecycle
- Internal company interactions and coordination
- Variations system and procedures
- Electronic lifecycle management
- Safety-related obligations and labelling
| Veranstaltungs-Code | FB24-486991-61077339 |
Bildungsziel der Schulung:
This seminar provides a comprehensive overview of all maintenance activities in the lifecycle of a medicinal product.
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Participants will receive thorough training on the main regulatory duties, from dossier update and variations to PV activities, through to labelling maintenance duties. All in a single seminar.
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Time and deadline management, as well as internal company interactions and coordination will be covered, which makes the seminar interesting for professionals from the various departments involved in the product lifecycle.
Veranstaltungsort:
Online-Webinar
weitere Orte/Termine
Kursart:
Online-Webinar
Kostenlos Info anfordern
