Medicinal products - Latest updates

Public consultation on the principles and guidelines of good manufacturing practice for active substances in medicinal products for human use -…

Implementing 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