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This review argues that their convergence represents a significant and timely opportunity. LAT development is constrained by a preclinical toolbox that fails to capture the coupled, tissue\u2010dependent processes, depot formation, sustained release, interstitial transport, host response, and local clearance that govern long\u2010acting performance in vivo. OoC platforms can reproduce the physiological microenvironments in which these processes unfold, including barrier structure, controlled perfusion, mechanical cues, and multicellular organization, under reproducible in vitro conditions. This review first maps the scientific and translational challenges of LAT development and the mechanistic requirements any preclinical platform must address. It then shows how the core design principles of OoC technology enable tissue\u2010mimicking platforms that reproduce the microenvironments of the main LAT administration routes. Finally, it brings the two fields together, mapping each LAT requirement directly onto a specific OoC capability, showing that the challenges of scale and long\u2010term culture stability are tractable through defined mitigation strategies, and setting out how the standardization and regulatory alignment now underway can position OoC platforms as credible decision\u2010support tools that complement, rather than replace, existing in vitro release models.<\/jats:p>","DOI":"10.1002\/adhm.71625","type":"journal-article","created":{"date-parts":[[2026,8,22]],"date-time":"2026-08-22T05:36:42Z","timestamp":1787377002000},"update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":0,"title":["Making the Case for Organ\u2010on\u2010Chip Platforms in Long\u2010Acting Therapeutics Development"],"prefix":"10.1002","volume":"15","author":[{"given":"Charlie","family":"Gowans","sequence":"first","affiliation":[{"name":"Division of Pharmacy and Optometry 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