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During the 2020-23 COVID-19 public health emergency, the European Medicines Agency (EMA) provided guidance for medicine developers and pharmaceutical companies to help speed up development and approval for COVID-19 medicines and address regulatory challenges arising from the pandemic.
HumanCOVID-19Clinical trialsCompassionate useRegulatory and procedural guidanceMedicine shortagesResearch and developmentScientific advice
HumanRegulatory and procedural guidanceResearch and developmentScientific guidelinesVaccines
NewsHumanCOVID-19Research and developmentVaccines
EventHumanMedicine shortagesResearch and development
Press releaseHumanCOVID-19Clinical trialsQuality of medicinesResearch and developmentVaccines
Press releaseHumanCOVID-19MedicinesResearch and developmentVaccines
NewsHumanCOVID-19MedicinesResearch and developmentVaccines
Press releaseHumanCOVID-19Clinical trialsResearch and developmentVaccines
NewsHumanVeterinaryCOVID-19Research and developmentVaccines
EventHumanPharmacovigilanceResearch and developmentVaccines