publicEuropean Medicines Agency · European Union · Updated Jul 21, 2026
Mandatory Use of PLM Portal eAF for CAP Variations
Marketing authorization holders must transition to the updated PLM Portal eAF by the mandatory deadline of September 1, 2026, ensuring correct submission of variations, particularly those related to pharmacovigilance.
Country ComplianceRegulatory Intelligence Lead
SOP Impact1 SOPs
ConfidenceHigh
Relevant for: Regulatory Intelligence Lead, QPPV
verifiedRegulatory action: Procedural Notice / Release Notes
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