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EMA evaluates applications for marketing authorisation submitted via the centralised procedure monitors the safety of medicines across their lifecycle and provides information to healthcare

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The EMA was founded after more than seven years of negotiations among EU governments and replaced the Committee for Proprietary Medicinal Products and the Committee for Veterinary

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Stronger Partnerships Cleaner Towns Environmental Management Agency EMA applauds Beitbridge Municipality for diligently seizing the opportunity availed through the Harare Beitbridge Highway

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EMA Lupane State University Celebrating Cultural heritage National World Wetlands Day 2026 commemoration Zimbabwe Commemorates World Environment Day at Mukuvisi Woodlands

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Get to know the EMA Stewards of Trinidad and Tobago s natural resources and environment

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EMA drug regulation and approval news Danish pharma major Novo Nordisk late yesterday announced that the European Commission EC has granted marketing authorization for

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The European Medicines Agency EMA is the central regulatory body responsible for the scientific evaluation supervision and safety monitoring of medicinal products across the European Union EU

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EMA s safety committee PRAC has confirmed its recommendation to limit the use of high strength creams containing 100 micrograms gram 0 01 of