Quality
Standards applied from fill to final carton
Every presentation in the range moves through the same four control stages, so the product a clinician opens matches the specification published for it.
01
Formulation & fill
Sterile filling under controlled classified conditions, with checks on concentration, fill weight and closure integrity for every batch.
02
Device assembly
Pens are assembled and tested for dial accuracy, dose window legibility and terminal cap retention before cartoning.
03
Serialisation
Each carton carries a unique identifier alongside batch and expiry data, positioned consistently across the portfolio for rapid verification.
04
Cold chain
Distribution is specified for 2 to 8 °C with light protection throughout. Cartons are designed to keep temperature sensitive contents shielded in transit.
Portfolio specifications
Storage2 to 8 °C, do not freeze
Light protectionOpaque carton board
ClosureTamper evident, first opening indicator
TraceabilityBatch, expiry and unique identifier
LabellingStrength, volume and route on principal panel
Use designationSingle patient presentations