Marburg Medium is the cornerstone of pharmaceutical Braille specification worldwide. Developed to deliver consistent tactile readability across languages, substrates and production methods, it defines the spatial geometry that makes compliant Braille … [Read more...]
Achieving Consistent Braille Legibility Across Packaging Substrates
Introduction: The challenge of maintaining consistency across diverse substrates Tactile legibility is the primary performance measure for compliant pharmaceutical Braille. Yet achieving consistent results across folding cartons, laminated labels, … [Read more...]
EU Accessibility Act 2025: What It Means for Braille on Medicinal Packaging
Introduction The European Accessibility Act (EAA) — Directive (EU) 2019/882 — applies across the EU from 28 June 2025. It harmonises accessibility requirements for a wide set of products and services in the internal market, driving a step-change … [Read more...]
Are you ready for Unified English Braille?
What is Unified English Braille? Unified English Braille (UEB) is an English language braille code standard, developed to permit representing the wide variety of literary and technical material in use in the English-speaking world today, in uniform … [Read more...]
Arabic Braille required on packaging of Medicines produced in UAE
New legislation for United Arab Emirates requires pharmaceutical companies to state the name and concentration of medicines in braille on all packaging produced for the UAE market. The braille must be included on the packs in Arabic braille and … [Read more...]
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