Selecting the optimal drug delivery device—whether vial and syringe, prefilled syringe, autoinjector, or wearable—demands a systematic technical assessment early in product development. Key multi-factors criteria such as dosage and dose volume, drug properties, user requirements, manufacturability and regulatory requirements all drive device suitability.
In this session, EdgeOne Medical discuss a structured methodology for comparative technical assessment, emphasizing critical elements, practical decision frameworks, and risk trade-off analysis for selecting the delivery system that best aligns with patient, product, and program objectives.
