Guideline on The Readability of The Labelling and Package Leaflet of Medicinal Products for Human Use
23 July 2010The guideline on the readability of labelling of medicinal products published by the European Commission in 2009 aims to ensure that the information on labelling and packaging is accessible and can be understood for safe use.
Legislation requires medicinal products to be accompanied by outer and/or immediate packaging information and a package leaflet.
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Guideline on The Readability of The Labelling and Package Leaflet of Medicinal Products for Human Use
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