A new sub-section launch within the section Documentation upgrading: Instructions for marketing authorisation holders for implementing the Braille script on the packaging of medicinal products
04.01.2013
The Agency for Medicinal Products and Medical Devices has launched on its webpages a new sub-section within the section Documentation upgrading (in Croatian), entitled Instructions for marketing authorisation holders for implementation of the Braille script on the product packaging (in Croatian).
The instruction entitled Documentation upgrading and an additional Instruction for submitting applications for documentation upgrading (in Croatian) has already been published within the same section.
Instructions for readability testing of the package leaflet will be published in this section of HALMED’s webpages in due time.
