A large area of the facility is dedicated to the packaging and labeling for investigational drugs

• Label text set up according to regulatory requirements
• Label design based on the packaging needs of the clinical study
• Mono-language / bi-language / multi-language labeling
• Procedures aimed at avoiding mixing between different products
• Re-labeling in case of changes (e.g.changes to the protocol, new “expiration date”, etc…)
• Possibility of tear-off label to document the dispensing of the product to the clinical site
• Use of booklets, provided by qualified external partners and overprinted with variable data on site