Medical Writing in Pharmacovigilance - Update your PV writing skills with numerous exercises!
Enhance your skills in writing key pharmacovigilance safety documents. In this two-day online seminar, you will gain a comprehensive understanding of the regulatory requirements and hands-on experience in crafting and maintaining PSUR, RMP, and DSUR. Learn best practices, avoid common pitfalls, and address global challenges to become a proficient Pharmacovigilance Writer!
- Best practices, common pitfalls, and cultural challenges in pharmacovigilance writing
- PV documents throughout the life cycle of a medicinal product: DSUR, RMP, and PSUR
- Safety concerns and their role in PV documents
- The role of the pharmacovigilance writer in an interdisciplinary team
- Practical exercises and lively discussions
| Veranstaltungs-Code | FB24-73760-61077505 |
Bildungsziel der Schulung:
This two-day online seminar will provide you with a solid understanding of essential pharmacovigilance documents, including the development safety update report (DSUR), periodic safety update report (PSUR), and risk management plan (RMP). You will learn how to create and update these documents across the life cycle of a medicinal product, ensuring compliance with global regulatory requirements. The course covers key regulatory obligations and common challenges in pharmacovigilance writing.
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Through practical exercises, you will enhance your writing skills and gain confidence in addressing the complexities of safety documentation. By the end of the seminar, you will be equipped to produce high-quality pharmacovigilance documents, tailored to meet industry standards and best practices. Become a proficient Pharmacovigilance Writer now!
Veranstaltungsort:
Online-Webinar
weitere Orte/Termine
Kursart:
Online-Webinar
Kostenlos Info anfordern
