This brief explores the rapid growth of home-use medical technologies driven by patient preference, digital health innovation, and healthcare system pressures. It examines regulatory, clinical, and operational considerations unique to home-based devices, including usability, safety, training, and post-market surveillance. IQVIA highlights the importance of real-world data, human-centered design, and proactive regulatory planning to support safe adoption. The brief positions home-use technologies as a key driver of decentralized care, improved access, and patient empowerment when supported by robust evidence and lifecycle management.

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