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市场调查报告书
商品编码
1852896
近身通讯市场(按应用、节点类型、通讯技术和频宽)——2025-2032 年全球预测Body Area Network Market by Application, Node Type, Communication Technology, Frequency Band - Global Forecast 2025-2032 |
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预计到 2032 年,近身通讯市场规模将达到 340.9 亿美元,复合年增长率为 10.27%。
| 主要市场统计数据 | |
|---|---|
| 基准年2024年 | 155.8亿美元 |
| 预计2025年 | 171.9亿美元 |
| 预测年份:2032年 | 340.9亿美元 |
| 复合年增长率(%) | 10.27% |
体域网路(BAN)技术正在重塑临床、国防和消费领域生理数据的采集、传输和利用方式。低功耗无线技术、小型化感测器和嵌入式处理技术的进步正在融合,实现可在穿戴式、可摄入和可植入节点上运行的连续监测系统。这些系统与更广泛的健康资讯基础设施的互通性日益增强,使得数据能够近乎即时地从个人设备流向远距医疗平台和分析引擎。
随着普及速度加快,BAN生态系统正从简单的健身追踪器扩展到慢性病管理、远端患者监护、远端医疗以及关键任务士兵追踪等领域。其底层技术包括工作在不同频宽的有线和无线通讯方案,每个频段的选择都兼顾了功耗、链路可靠性和合规性。同时,材料科学和生物相容性的创新正在延长设备的使用寿命并提高患者的舒适度,而边缘运算和安全韧体使得用户能够在更靠近感测器来源的位置获得可操作的洞察。
本执行摘要重点阐述技术选择、监管动态和地缘政治变化如何影响供应链、产品蓝图和商业模式,并提炼这些趋势对产业相关人员的战略意义。其目的是帮助领导者清晰了解当前动态,并为支援稳健成长和临床效用的近期决策提供切实可行的指南。
近身通讯)领域正经历多重变革,这些变革共同重塑了产品设计重点、合作伙伴生态系统和监管方式。首先,不可否认的是,单一用途设备正向融合生理、生化和情境资料流的多模态感测平台转变。这项转变的驱动力来自临床对更丰富的纵向资料集的需求,这些资料集有助于提高诊断准确性和治疗监测效果;以及消费者对统一化、侵入性较小的穿戴式装置的偏好。
其次,连接模式正在不断演变。设计人员会根据特定应用场景的权衡取舍(例如通讯、功耗以及与其他无线系统的共存性)来选择频宽和通讯技术。这促进了模组化架构的发展,使得通讯模组可以互换,从而加快技术更新周期,而无需对设备进行彻底的重新设计。第三,资料管治和网路安全的考量日益凸显,成为采购需求中的重中之重,推动了对安全启动、加密远端检测和身分管理等方面的投资,以维护边缘、网关和云端的资料完整性。
最后,经营模式正转向基于结果和订阅的模式,将分析和服务与设备硬体捆绑在一起。这项变更影响着收益确认和售后服务义务,并促使设备製造商与软体供应商、云端託管商和临床整合商建立更深入的伙伴关係。总而言之,这些变化正在加速跨学科合作,并提升系统层级检验和长期临床证据的重要性。
2025年美国关税环境将对人体区域网路(BAN)供应链、筹资策略和区域采购决策产生多重影响。关税调整将影响感测器、微控制器、天线和专用基板组件的经济效益,并可能改变亚洲、美洲和欧洲等地製造地的相对吸引力。为此,製造商正在重新审视垂直整合方案,探索近岸组装以降低成本波动并缩短前置作业时间,并重新设计材料清单,尽可能优先选择国内可获得的替代产品。
同时,采购团队和合约製造商正在协商更长期的供应商协议,并加入灵活的采购条款,以应对关税造成的价格波动。对成本敏感的设计可能会优先考虑减少零件数量、采用标准化通讯模组和延长使用寿命,以在不牺牲合规性或设备安全性的前提下保护净利率。监管进口限制和关税分类也促使监管团队和供应链团队密切合作,以确保统一的关税表与医疗设备的分类和豁免条款相符。
从策略角度来看,积极建立关税情境模型并实施适应性筹资策略的企业,更有利于维持产品供应的连续性并维护客户关係。诸如双重采购和在地化检验能力等跨职能紧急应变计画,能够降低政策突变带来的风险,即使在价格压力下,也能支持企业持续进行创新投资。
细分领域的动态变化揭示了不同应用、节点类型、通讯技术和频宽分类所带来的机会和技术限制。在众多应用中,医疗保健领域,例如慢性病管理、远端患者监护和远距医疗,对临床级远端检测和检验的演算法的需求最为迫切。慢性病管理主要关注糖尿病、高血压和呼吸系统监测,这些领域需要持续的生化和生理讯号。同样,远端医疗远端患者监护优先考虑心血管、血糖和神经系统监测模式,这些模式需要高数据保真度和低延迟传输;而远端医疗越来越多地利用远距离诊断和虚拟咨询工作流程来扩大临床医生的服务范围。军事和国防应用着重于战备追踪和士兵监测,前者强调模拟诊断和损伤预测能力,后者则着重于在极端环境压力下监测疲劳和生命征象。在运动和健身领域,睡眠和压力监测等健康功能与运动员表现追踪和运动监测并存,这促使消费者对产品的耐用性和可操作的指导建议都抱有更高的期望。
植入式设备,例如心臟植入、药物传输系统和神经刺激设备,必须满足最高的生物相容性和可靠性标准;而可摄入式节点,例如胶囊相机和pH感测器,则优先考虑瞬态运作和安全排泄。穿戴式节点,例如健身手环、智慧服装和智慧型手錶,则需要在感测精度、人体工学和电池续航时间之间取得平衡。有线和无线通讯技术的选择反映了抗干扰能力、功耗预算以及与临床工作流程整合的便利性之间的权衡。 2.4 吉赫频段的解决方案通常利用蓝牙或Wi-Fi实现普遍连接,而400 MHz频段则支援远距离穿透特性,适用于植入式通讯和某些业余无线电应用。超宽频(UWB)版本提供精确测距,并提供远距和短距离UWB选项,以满足定位感知应用场景的需求。总而言之,这些细分可以透过将技术限制与最终用户需求和部署环境相匹配,为产品蓝图和监管策略提供资讯。
美洲、欧洲、中东和非洲以及亚太地区的动态变化正以不同的方式影响医疗设备的应用路径、监管时间表和供应链韧性。在美洲,监管机构和医疗系统正在推动对能够与现有电子健康记录设施整合的远端监测解决方案的需求,而商业性支付方和雇主则在探索基于价值的报销模式,以奖励已证实的临床疗效和成本节约。这种环境正在促进设备製造商和医疗系统整合商之间的伙伴关係,并鼓励对强大的隐私保护和互通性功能进行投资。
在欧洲、中东和非洲,监管协调和资料保护条例的实施,为医疗器材认证和跨境资料流动建构了一个复杂但可行的环境。欧洲的相关人员经常强调严格的临床检验和对区域医疗器材标准的遵守,这不仅提高了市场进入门槛,也增强了医疗服务提供者之间的信任。中东和非洲的医疗器材普及情况不尽相同,都市区医疗系统普及迅速,而偏远地区则面临基础设施的限制。
亚太地区拥有庞大的人口基数、快速发展的远距远端医疗系统和大规模的製造能力,因此蕴藏着多元化的机会。监管审批流程在不同地区可能存在显着差异,当地的製造激励措施和关税政策也会影响企业选择在何处进行组装和最终测试。因此,具有策略眼光的企业正在将本地化的临床证据产生与可扩展的部署模式相结合,以加速技术应用,同时应对区域合规性和供应链的复杂性。
人体区域网路领域的竞争格局由多种实体共同塑造,包括半导体供应商、纯粹的感测器製造商、医疗设备原始设备製造商 (OEM)、连接晶片组供应商、软体分析公司和系统整合。半导体和射频组件供应商是关键推动者,他们提供低功耗无线电、微控制器和整合式收发器,这些组件限制了电池寿命和通讯可靠性。感测器製造商提供灵敏的生化和生理模组,这些模组支撑着临床效用,他们的蓝图影响着新的医疗功能和监管申报的时间表。
医疗设备製造商正透过整合解决方案实现差异化,这些解决方案将经过检验的感测技术与临床工作流程和报销途径相结合。连接供应商则专注于互通性,提供可简化多频宽和通讯标准认证的协定堆迭和参考设计。软体和分析公司正在将远端检测转化为具有临床意义的洞察,而成功的公司则在检验的演算法、可解释性和符合监管要求的文件方面投入巨资。系统整合和契约製造在扩大生产规模、管理供应链复杂性以及支援设备生命週期服务(包括韧体更新和网路安全修补程式)方面发挥着至关重要的作用。
有效竞争的关键在于展现端到端的价值:可靠的感测、安全合规的连结、有意义的分析以及营运支援。策略伙伴关係关係、智慧财产权保护和经临床验证的成果是买家在选择供应商和合作伙伴时评估的关键差异化因素。
产业领导者应优先考虑一系列切实可行的倡议,以保障利润、加速临床应用并确保产品系列面向未来。首先,投资于模组化架构,将感测、处理和通讯元件解耦,使各组件能够根据频率分配的变化、新的低功耗无线标准以及资费调整进行独立昇级。这种模组化设计可降低重新设计成本,并加速渐进式创新产品的上市速度。其次,从产品开发的早期阶段就实施严格的网路安全和隐私保护设计,以满足监管要求并维护相关人员的信任。
第三,我们将寻求策略性的双源采购和区域製造伙伴关係,以确保供应链的灵活性,并降低关税波动和物流中断带来的营运风险。第四,我们将开发以结果为导向的服务,将设备与分析、临床工作流程优化和报销改进相结合,以建立稳定、持续的收益来源,并展现可衡量的临床价值。第五,我们将投资产生长期临床证据和真实世界绩效数据,以支持与支付者的沟通和监管申报。
最后,与云端服务供应商、医疗保健系统、国防机构和运动表现团体建立跨领域合作伙伴关係,以加速部署并共同开发针对特定领域最佳化的解决方案。这些伙伴关係关係应遵循明确的智慧财产权、资料共用和商业化条款,以确保公平并保护未来的竞争优势。
本执行摘要的调查方法结合了访谈、技术文献综述和跨学科检验,旨在揭示近身通讯)的现状。主要资讯来源包括对设备工程师、法规事务负责人、采购负责人、临床终端用户以及国防和体育专案经理的结构化访谈,以收集关于技术限制、部署挑战和采购考虑的第一手观点。这些定性见解与同行评审的技术出版物、标准文件和官方监管指南进行了交叉核对,以确保其符合当前的合规要求和工程最佳实践。
技术评估重点在于植入式、可摄入式和穿戴式装置的装置架构、无线共存策略、频宽特性以及节点特定的可靠性考量。供应链和商业分析考虑了采购模式、关税影响和生产弹性。透过审查临床试验设计、真实世界证据倡议和支付方参与框架,评估了证据要求和临床检验方法。与独立专家和从业人员的同行检验完善了关键假设,并突出了切实可行的缓解策略。
在整个调查方法中,可追溯性和透明度至关重要,我们记录了资讯来源和假设,以便将建议与证据和实践者的证词直接对应。这种方法既支持组织进行策略规划,也支持其将研究成果应用于实际营运。
总之,体域网路代表着一项关键的技术前沿,对医疗保健、国防战备和消费者福祉有广泛的影响。微型化感测、先进的无线技术和边缘分析的融合,能够实现连续、情境丰富的监测,从而将零散的互动转化为长期的护理和性能优化。然而,要充分发挥这一潜力,需要精心协调设计选择、符合监管要求、确保供应链的韧性以及收集证据,以满足临床和商业相关人员的需求。
采用模组化架构、优先考虑网路安全并建立健全的临床检验程序的组织将更有利于把握未来的机会。同样重要的是,组织能够透过灵活的采购和区域製造策略来应对地缘政治和政策变化,例如关税调整。从半导体供应商到临床医生再到系统整合商,整个生态系统的协作将加速技术的应用,同时确保解决方案的安全、可靠和互通性。
最终,实现可扩展且永续的BAN部署之路,将以严谨的工程设计、可靠的证据以及能够协调支付方、医疗服务提供方和最终用户之间奖励的商业性可行服务模式为基石。那些在这些优先事项上采取果断行动的人,将为下一代互联医疗和绩效系统树立标竿。
The Body Area Network Market is projected to grow by USD 34.09 billion at a CAGR of 10.27% by 2032.
| KEY MARKET STATISTICS | |
|---|---|
| Base Year [2024] | USD 15.58 billion |
| Estimated Year [2025] | USD 17.19 billion |
| Forecast Year [2032] | USD 34.09 billion |
| CAGR (%) | 10.27% |
Body Area Network (BAN) technologies are reshaping how physiological data is captured, transmitted, and acted upon in clinical, defense, and consumer settings. Advances in low-power radios, miniaturized sensors, and embedded processing have converged to enable continuous monitoring systems that operate across wearable, ingestible, and implantable nodes. These systems are increasingly interoperable with broader health information infrastructures, allowing data to flow from personal devices to remote care platforms and analytics engines in near real time.
As adoption accelerates, the BAN ecosystem is expanding beyond simple fitness trackers to encompass chronic disease management, remote patient monitoring, telemedicine capabilities, and mission-critical soldier tracking. The underlying technologies include a mix of wired and wireless communication approaches operating within varied frequency bands, each chosen to balance power consumption, link reliability, and regulatory compliance. Concurrently, innovations in materials science and biocompatibility are extending device longevity and patient comfort, while edge compute and secure firmware are enabling actionable insights to be derived closer to the sensor source.
This executive summary distills the strategic implications of these trends for industry stakeholders, focusing on how technology choices, regulatory dynamics, and geopolitical shifts are influencing supply chains, product roadmaps, and commercial models. The intent is to equip leaders with a clear understanding of current dynamics and pragmatic guidance for near-term decisions that support resilient growth and clinical utility.
The landscape for Body Area Networks is undergoing multiple transformative shifts that collectively redefine product design priorities, partner ecosystems, and regulatory approaches. First, there is an unmistakable movement from single-purpose devices toward multi-modal sensing platforms that combine physiological, biochemical, and contextual data streams. This shift is driven by clinical demand for richer longitudinal datasets that improve diagnostic confidence and therapeutic monitoring, and by consumer preference for unified, less obtrusive wearables.
Second, connectivity paradigms are evolving: designers are selecting frequency bands and communication technologies based on use-case-specific trade-offs between range, power, and coexistence with other wireless systems. This has encouraged modular architectures that allow for interchangeable communication modules, enabling faster technology refresh cycles without full device redesign. Third, data governance and cybersecurity considerations are rising to the top of procurement requirements, prompting investments in secure boot, encrypted telemetry, and identity management to maintain data integrity across edge, gateway, and cloud layers.
Finally, business models are shifting toward outcomes-based and subscription approaches, where device hardware is bundled with analytics and services. This change is affecting revenue recognition and aftercare obligations, and it is prompting device makers to forge deeper partnerships with software vendors, cloud hosts, and clinical integrators. Taken together, these shifts are accelerating cross-disciplinary collaboration and elevating the importance of system-level validation and longitudinal clinical evidence.
The tariff environment in the United States during 2025 imposes a layered influence on Body Area Network supply chains, procurement strategies, and regional sourcing decisions. Tariff adjustments affect component-level economics for sensors, microcontrollers, antennas, and specialty substrates, and they can alter the relative attractiveness of manufacturing footprints across Asia, the Americas, and Europe. In response, manufacturers are reassessing vertical integration options, considering near-shore assembly to mitigate cost volatility and shorten lead times, and redesigning bills of materials to favor domestically available alternatives when feasible.
At the same time, procurement teams and contract manufacturers are negotiating longer-term supplier agreements and incorporating flexible sourcing clauses to absorb tariff-induced price movement. This has downstream effects on product roadmaps, where cost-sensitive designs may prioritize reduced part counts, unified communications modules, or longer-lived components to preserve margin without sacrificing regulatory compliance or device safety. Regulatory import controls and tariff classifications are also prompting closer collaboration between regulatory affairs and supply chain teams to ensure that harmonized tariff schedules align with medical device classifications and exemptions.
From a strategic vantage point, organizations that proactively model tariff scenarios and implement adaptive sourcing strategies are better positioned to preserve product continuity and protect customer relationships. Cross-functional contingency planning, including dual-sourcing and localized validation capabilities, reduces exposure to sudden policy shifts and supports sustained investment in innovation even under pricing pressure.
Segment-level dynamics reveal differentiated opportunities and technical constraints across application, node type, communication technology, and frequency band categorizations. Within applications, medical use cases such as chronic disease management, remote patient monitoring, and telemedicine exhibit the greatest demand for clinical-grade telemetry and validated algorithms; chronic disease management itself concentrates attention on diabetes, hypertension, and respiratory monitoring where continuous biochemical and physiological signals are essential. Similarly, remote patient monitoring prioritizes cardiovascular, glucose, and neurological monitoring modalities that demand high data fidelity and low-latency transmission, while telemedicine increasingly leverages remote diagnostics and virtual consultation workflows to extend clinician reach. Military and defense applications emphasize combat readiness tracking and soldier monitoring, with the former relying on simulation diagnostics and injury prediction capabilities and the latter focusing on fatigue and vital sign monitoring under extreme environmental stresses. In the sports and fitness domain, health and wellness features such as sleep and stress monitoring coexist with performance tracking for athletes and exercise monitoring, creating consumer expectations for both durability and actionable coaching insights.
Node type considerations drive form factor and certification decisions: implantable devices such as cardiac implants, drug delivery systems, and neurostimulators must meet the highest biocompatibility and reliability standards, whereas ingestible nodes like capsule cameras and pH sensors emphasize transient operation and safe excretion. Wearable nodes, including fitness bands, smart clothing, and smart watches, balance ergonomics and battery life against sensing fidelity. Communication technology choices between wired and wireless implementations reflect trade-offs in interference resilience, power budgets, and ease of integration into clinical workflows. Frequency band selection further refines these trade-offs: 2.4 gigahertz solutions often leverage Bluetooth or Wi-Fi for ubiquitous connectivity, 400 megahertz bands support longer penetration characteristics suited to implantable communications and certain amateur radio applications, and UltraWideband variants offer precise ranging with both long-range and short-range UWB options for location-aware use cases. Collectively, these segmentation dimensions inform product roadmaps and regulatory strategies by aligning technical constraints with end-user needs and deployment environments.
Regional dynamics shape adoption pathways, regulatory timelines, and supply chain resilience in distinct ways across the Americas, Europe, Middle East & Africa, and Asia-Pacific. In the Americas, regulatory authorities and health systems are driving demand for remote monitoring solutions that integrate with established electronic health record infrastructures, while commercial payers and employers are exploring value-based reimbursement models that reward demonstrable clinical outcomes and cost reductions. This environment favors partnerships between device makers and health-system integrators, and it encourages investment in robust privacy and interoperability features.
Across Europe, the Middle East, and Africa, regulatory harmonization and data protection regulations create a complex but navigable landscape for device certification and cross-border data flows. European stakeholders frequently emphasize rigorous clinical validation and adherence to regional device standards, which raises the bar for market entry but also supports strong trust among healthcare providers. In the Middle East and Africa, adoption is heterogeneous, with pockets of rapid deployment in urban health systems paired with infrastructure constraints in remote settings; solutions that offer offline data capture and low-bandwidth synchronization show particular promise.
Asia-Pacific presents a diverse set of opportunities driven by large population bases, rapidly expanding telehealth ecosystems, and significant manufacturing capacity. Regulatory timelines can vary markedly across jurisdictions, and local manufacturing incentives or tariff policies influence where companies choose to locate assembly and final testing. Strategic players are therefore combining localized clinical evidence generation with scalable deployment models to accelerate adoption while managing regional compliance and supply chain complexity.
Competitive dynamics in the Body Area Network space are shaped by a spectrum of organizations that include semiconductor suppliers, specialized sensor manufacturers, medical device OEMs, connectivity chipset vendors, software analytics firms, and systems integrators. Semiconductor and RF component suppliers are critical enablers, delivering low-power radios, microcontrollers, and integrated transceivers that set constraints on battery life and communication reliability. Sensor manufacturers that provide high-sensitivity biochemical and physiological modules underpin clinical utility, and their roadmaps influence the cadence of new medical features and regulatory submissions.
Medical device original equipment manufacturers are differentiating through integrated solutions that combine validated sensing with clinical workflows and reimbursement pathways. Connectivity vendors are focused on interoperability, delivering stacks and reference designs that simplify certification across multiple frequency bands and communication standards. Software and analytics companies translate raw telemetry into clinically actionable insights, and those that succeed are investing heavily in validated algorithms, explainability, and regulatory-grade documentation. Systems integrators and contract manufacturers play an essential role in scaling manufacturing, managing supply chain complexity, and supporting device lifecycle services including firmware updates and cybersecurity patches.
Effective competition hinges on the ability to demonstrate end-to-end value, spanning reliable sensing, secure and compliant connectivity, meaningful analytics, and operational support. Strategic partnerships, IP protection, and demonstrated clinical outcomes are the primary differentiators that buyers evaluate when selecting suppliers and collaborators.
Industry leaders should prioritize a set of actionable initiatives to protect margin, accelerate clinical adoption, and future-proof product portfolios. First, invest in modular architectures that decouple sensing, processing, and communication elements so that components can be upgraded independently in response to evolving frequency allocations, new low-power radio standards, or changes in tariff exposures. This modularity reduces redesign costs and shortens time-to-market for incremental innovations. Second, embed rigorous cybersecurity and privacy-by-design practices early in product development to meet escalating regulatory expectations and to preserve stakeholder trust; security features should be validated through independent third-party testing and documented for procurement teams.
Third, pursue strategic dual-sourcing and regional manufacturing partnerships to create supply chain flexibility and to mitigate the operational risk introduced by tariff shifts or logistic disruptions. Fourth, develop outcome-oriented service offerings that bundle devices with analytics, clinician workflows, and reimbursement enablement to create sticky, recurring revenue streams and to demonstrate measurable clinical value. Fifth, invest in the generation of longitudinal clinical evidence and real-world performance data that supports payer conversations and regulatory submissions; evidence generation is increasingly decisive in procurement decisions.
Finally, cultivate cross-sector alliances with cloud providers, healthcare systems, defense agencies, and sports performance groups to accelerate deployment and to co-develop domain-optimized solutions. These partnerships should be governed by clear IP, data-sharing, and commercialization terms to ensure fairness and to protect future competitive advantage.
The research methodology for this executive summary combined primary interviews, technical literature synthesis, and cross-disciplinary validation to build a robust picture of the Body Area Network landscape. Primary inputs included structured interviews with device engineers, regulatory affairs leads, procurement officers, clinical end-users, and defense and sports program managers to gather firsthand perspectives on technical constraints, deployment challenges, and procurement considerations. These qualitative insights were triangulated against peer-reviewed technical publications, standards documentation, and public regulatory guidance to ensure alignment with current compliance expectations and engineering best practices.
Technical evaluation emphasized device architecture, wireless coexistence strategies, frequency band characteristics, and node-specific reliability considerations for implantable, ingestible, and wearable devices. Supply chain and commercial analyses examined sourcing patterns, tariff influences, and manufacturing flexibility. Evidence requirements and clinical validation approaches were assessed through review of clinical study designs, real-world evidence initiatives, and payer engagement frameworks. Cross-validation with independent subject-matter experts and practitioners helped refine key assumptions and surface pragmatic mitigation strategies.
Throughout, the methodology prioritized traceability and transparency, documenting sources and assumptions so that recommendations can be directly mapped to evidence and practitioner testimony. This approach supports both strategic planning and operational implementation for organizations seeking to act on the insights presented.
In conclusion, Body Area Networks represent a pivotal technology frontier with broad implications across healthcare delivery, defense readiness, and consumer wellbeing. The convergence of miniaturized sensing, advanced wireless options, and edge analytics is enabling continuous, context-rich monitoring that transforms episodic interactions into longitudinal care and performance optimization. However, realizing this potential requires careful orchestration of design choices, regulatory alignment, supply chain resilience, and evidence generation to satisfy clinical and commercial stakeholders.
Organizations that adopt modular architectures, prioritize cybersecurity, and build robust clinical validation programs will be best positioned to capture the opportunities ahead. Equally important is the ability to respond to geopolitical and policy shifts-such as tariff changes-through adaptive sourcing and regional manufacturing strategies. Collaboration across the ecosystem, from semiconductor suppliers to clinicians and integrators, will accelerate adoption while ensuring that solutions remain safe, reliable, and interoperable.
Ultimately, the path to scalable, sustainable BAN deployments is paved by disciplined engineering, rigorous evidence, and commercially viable service models that align incentives across payers, providers, and end users. Those who act decisively on these priorities will set the standards for the next wave of connected health and performance systems.