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EventHumanMedicinesResearch and development
EventHumanMedicinesResearch and development
HumanRegulatory and procedural guidanceMedicinesResearch and development
Medicine post-authorisationVeterinary
NewsHumanMedicinesResearch and development
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
MedicineHumanWithdrawn application
HumanCOVID-19Clinical trialsCompassionate useRegulatory and procedural guidanceMedicine shortagesResearch and developmentScientific adviceVaccines
Press releaseHumanCOVID-19MedicinesResearch and development
EventHumanMedicine shortagesResearch and development