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Medicinal products - Latest updates (313)
RSSImplementing act on the requirements for the assessment of the regulatory framework applicable to the manufacturing of active substances of medicinal…
Volume 9B of The Rules Governing Medicinal Products in the European Union – Guidelines on Pharmacovigilance for Medicinal Products for Veterinary Use
Delegated act on the detailed rules for a unique identifier for medicinal products for human use, and its verification - Concept paper submitted for…
The European Commission adopts revised proposals setting out clearer rules on information on prescription-only medicines
Commission Call for Expression of Interest
Public consultation of the revised Commission guidelines on Good Distribution Practice of Medicinal Products for Human Use
New Directive on Falsified Medicines published in the Official Journal of the European Union
Press release: EU adopts ambitious measures to fight against falsified medicines
Press release: Traditional herbal medicines: more safety for products put on EU market
Paola Testori Coggi, Director-General of DG Health & Consumers, explains the Herbals Directive
Public consultation on a concept paper on an amendment of Commission Regulation (EC) No 658/2007 concerning financial penalties committed by…
Protecting patients: EU to upgrade medicine safety monitoring
EMA Agency publishes policy on communicating safety issues for human medicines