Launch of the new subsection “Instructions for marketing authorisation holders about the readability and simplicity testing of the package leaflet” within the section “Documentation upgrading for medicinal products” of our website
15.03.2013
A new subsection "Instructions for marketing authorisation holders about the readability and simplicity testing of the package leaflet” has been launched on the webpages of the Agency for Medicinal Products and Medical Devices within the section "Documentation upgrading of medicinal products”.
The instructions "Documentation upgrading”, additional ”Instruction for submitting applications for dossier upgrading” and "The instruction for marketing authorisation holders about the implementation of the Braille script on the packaging of medicinal products” have already been posted in this section (in Croatian).
