Regulatory Affairs and GMP compliance in Eastern Europe - Considerations for the EAEU and Non-EAEU markets
This online training offers comprehensive insights into Regulatory Affairs, CMC, and GMP requirements, with a focus on the latest updates and developments in EAEU countries.
- Regulatory Framework and Requirements
- Approval Processes and Documentation
- Product Management and Maintenance
- Quality Management and GMP Audits
- International Markets and Opportunities
| Veranstaltungs-Code | FB24-48547-61077522 |
Bildungsziel der Schulung:
This seminar is designed to provide a thorough understanding of the regulatory framework and practical requirements for the registration, maintenance, and variation of medicinal products in the Eurasian Economic Union (EAEU). It also addresses critical aspects such as compliance with GMP standards, handling specific requirements for biologicals, and exploring regulatory opportunities in non-EAEU markets.
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The seminar aims to equip participants with the knowledge and tools to manage applications, variations and audits efficiently while ensuring adherence to EAEU standards and guidelines.
Veranstaltungsort:
Online-Webinar
weitere Orte/Termine
Kursart:
Online-Webinar
Kostenlos Info anfordern
