GMP: New Concept Paper of the European Commission on the Use of Safety Features against Falsified Medicinal Products

On 18 November 2011, the European Commission published a concept paper entitled \"Delegated Act on the Detailed Rules for a Unique Identifier for Medicinal Products for Human Use, and its Verification\". The document refers to Directive 2011/62/EU which deals with safety features for medicinal products. The concrete implementation - which is expected for 2014 - will then be set out through so-called \"delegated acts\".