How should serialisation be implemented for ‘titration’ packs, only to outer box or it should also be applied to the inner boxes too?
Serialisation should be applied to the pack which is the unit of sale and to which the labelling provisions in Article 54 of Council Directive 2001/83/EC apply. In the case of titration packs where different strengths of a medicine are included in separate blister strips within a single outer carton, the single outer carton will be serialised.