GMP: New Concept Paper of the European Commission on the Use of Safety Features against Falsified Medicinal Products
07.12.2011
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 source of the news: http://www.gmp-compliance.org/eca_news_2866_7132.html
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