Secondary Packaging & Labeling
Eurofins CDMO (Contract Development & Manufacturing Organization) can perform customized labeling and secondary packaging of every clinical trial phases (I, II, III) for sterile and non-sterile dosage forms (blisters, blister-cards, vials, syringes, bottles, sachet etc…).
1 labels printing room, 5 suites at RT and 2 suites at 4°C are dedicated to this activity.
We are able to advise you on the optimal design of the patient kit accordingly to your protocol. Our project manager team can handle additional activities like randomization list creation, text translation, comparator sourcing and blinding, ancillary kits management (perfusion materials), leaflet printing…