EFPIA：2026年EFPIA和EAHP联合实施指南报告（英文版）

In collaboration with EAHP, a coalition of industry partners have discussed and agreed the concept of extending the existing medicinal pack coding, as exemplified by the Falsified Medicines Directive, to the unit dose level. The process would be applicable to many product presentations, e.g. vials, glass/plastic bottles, blisters, pre-filled syringes, pens, sachets, stick packs, ampoules, cartridges etc. where either multiple dose packages are provided or for combination products e.g. medicat