publicEuropean Medicines Agency · European Union · Updated Sep 17, 2026
Updated Timeline for Plasma Master File Submissions: Period 2026-2028
PV teams must review and update their workflows related to regulatory intelligence monitoring to align with the new PMF submission timelines and ensure compliance with upcoming guidelines specified in the 3-year work plan.
Country ComplianceRegulatory Intelligence Lead
SOP Impact1 SOPs
ConfidenceHigh
Relevant for: Regulatory Intelligence Lead
verifiedRegulatory action: Regulators
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