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HumanRegulatory and procedural guidanceRare diseasesResearch and development
HumanResearch and developmentScientific guidelines
VeterinaryRegulatory and procedural guidanceResearch and developmentScientific guidelines
ReferralHuman
HumanResearch and developmentScientific guidelines
EventHumanVeterinaryCorporateData on medicinesInnovationResearch and development
OrphanHuman
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
EventVeterinaryResearch and development
ReferralHuman