Fake invoices, emails or phone calls request payments in EMA’s name
How real-world evidence benefits medicines regulation
How EMA helps protect environment
PRAC carried out its responsibilities for managing risks associated with medicine use
Advice and guidance for manufacturers
Platform enables reporting on supply, demand and availability of medicines
Milestone highlights EMA's changing role in Europe
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Eco-Management and Audit Scheme (EMAS) certificate is a mark of environmental excellence in the EU
Outcomes of the Committee for Veterinary Medicinal Products (CVMP) meeting
PRAC carried out its broad range of responsibilities for managing the risks associated with medicine use
Manufacturers can request advice on their medical device clinical development programme
Clinical Trials Information System now supports submission, assessment and oversight of all trials in the EU
Eight new medicines recommended for approval; one positive opinion for a medicine intended for use outside the EU
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