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EMA (EU)
GUIDANCE FINAL
Concept paper on the revision of the guideline on data requirements for authorisation of immunological veterinary medicinal products in exceptional circumstances (EMA/CVMP/IWP/251947/2021)
Published: 6/26/2026Detected: 7/2/2026

Summary preview

Revises EMA/CVMP guidance for marketing-authorisation applications for immunological veterinary medicinal products under “exceptional circumstances,” aiming to reduce divergent interpretation and improve procedural…

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immunology
infectious_disease
rare_diseases
manufacturing
quality
clinical
safety
labeling
#exceptional circumstances
#immunological veterinary medicinal products
#veterinary vaccines

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