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𝗧𝗵𝗲 𝗠𝗮𝗿𝗸𝗲𝘁 𝗥𝗲𝗮𝗹𝗶𝘁𝘆 🔹 Chronic disease is driving an unstoppable shift toward patient self-administration — biologics that cannot be orally formulated must be injected, and patients expect devices that are intuitive, reliable and safe to use at home 🔹 Fewer than 14% of drugs make it from Phase I to commercial market — and usability gaps in combination products are increasingly cited in FDA Complete Response Letters, adding median delays of ~435 days before approval 🔹 Pharma clients are now enquiring about PFS formats and autoinjector options before IND-enabling studies even begin — device strategy is no longer a late-stage decision 🔹 In an increasingly competitive landscape, the delivery system is a differentiator
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