시장보고서
상품코드
1836848

처방 관리 소프트웨어 시장 : 구성요소, 전개 형태, 최종사용자, 용도, 조직 규모별 - 세계 예측(2025-2032년)

Prescription Management Software Market by Component, Deployment Mode, End User, Application, Organization Size - Global Forecast 2025-2032

발행일: | 리서치사: 360iResearch | 페이지 정보: 영문 197 Pages | 배송안내 : 1-2일 (영업일 기준)

    
    
    




■ 보고서에 따라 최신 정보로 업데이트하여 보내드립니다. 배송일정은 문의해 주시기 바랍니다.

처방 관리 소프트웨어 시장은 2032년까지 CAGR 17.48%로 43억 2,000만 달러로 성장할 것으로 예측됩니다.

주요 시장 통계
기준 연도 2024년 11억 9,000만 달러
추정 연도 2025년 13억 9,000만 달러
예측 연도 2032 43억 2,000만 달러
CAGR(%) 17.48%

처방전 관리 소프트웨어의 가치 제안, 임상 통합을 촉진하는 요인, 규제 압력, 업무상 이점을 소개하는 전략 개요

처방전 관리 소프트웨어의 상황은 임상 진료, 약국 업무, 의료 IT 인프라와 교차하여 투약 안전성, 워크플로우 효율성, 환자 경험에 중대한 영향을 미치고 있습니다. 이 주요 요약에서는 기술이 전자 의료 기록, 전자 처방전 네트워크, 약국 재고 시스템과 어떻게 통합되어 오류를 줄이고, 처방 워크플로우를 간소화하며, 복약 순응도 개입을 지원하는지 설명함으로써 처방 관리 솔루션의 핵심 가치 제안에 대해 설명합니다. 제안합니다. 의사결정자는 이러한 플랫폼을 분산된 진료 환경 전반에 걸쳐 임상의의 의도, 약사의 확인, 환자의 행동을 조정하는 결합 조직으로 간주해야 합니다.

또한 규제 및 상환 역학은 디지털 관리 및 데이터 기반 약물 관리를 점점 더 장려하고 있습니다. 그 결과, 상호운용성, 데이터 거버넌스, 임상의 중심의 설계를 우선시하는 조직은 운영상의 이점을 더 빠르게 얻을 수 있습니다. 이러한 맥락에서 기술의 역할은 트랜잭션 처리에 그치지 않고, 분석 중심의 스튜어드십, 타겟팅된 환자 접근, 안전 모니터링 등을 가능하게 합니다. 따라서 리더는 임상적 유용성과 기술적 견고성의 균형을 맞추고, 도입 전략을 통해 혼란을 완화하는 동시에 투약 결과를 측정 가능한 수준으로 개선해야 합니다.

마지막으로, 이 소개에서는 통합의 복잡성, 벤더의 생태계 상호운용성, 변경 관리의 필요성, 임상 경로와 기술 선택 간의 일치의 중요성 등 실무적인 고려 사항을 강조함으로써 보다 심층적인 분석을 위한 발판을 마련합니다. 다음 섹션에서는 이러한 토대 위에서 변화의 추세, 정책의 영향, 세분화의 뉘앙스, 지역 역학, 경쟁의 포지셔닝, 도입을 위한 실행 가능한 단계를 살펴봅니다.

AI를 활용한 의사결정 지원, 상호운용성 표준, 환자 중심의 디지털 워크플로우 등 처방전 관리를 재구성하는 혁신적인 힘

처방전 관리는 인공지능의 발전, 상호운용성 프레임워크의 확대, 환자 중심의 디지털 서비스에 대한 중요성 등으로 인해 혁신적인 변화를 겪고 있습니다. AI를 활용한 임상 판단 지원은 현재 문맥을 고려한 처방 제안, 처방을 고려한 대안, 경고 피로를 줄이면서 안전성을 우선시하는 자동 경고로 임상의를 지원하고 있습니다. 이러한 기능은 실시간 데이터 교환 표준 및 API와 결합하여 임상의, 약국, 지불자 간의 긴밀한 워크플로우를 가능하게 하고, 의도와 실행의 일치성을 향상시킵니다.

동시에 새로운 상호운용성 표준과 인증에 대한 기대는 통합의 마찰을 줄이고 데이터 이동성을 가속화하고 있습니다. 그 결과, 조직은 레거시 시스템을 완전히 대체하지 않고도 전자처방전 엔진, 재고 관리, 준수 도구를 연결하는 모듈식 접근 방식을 채택할 수 있습니다. 또한, 모바일 복약 순응도 도구, 텔레파마 서비스, 환자 포털로 대표되는 의료 IT의 소비자화는 복약 관리를 가정과 지역사회로 확대하는 새로운 접점을 창출하고 있습니다.

마찬가지로 가치 기반 치료 모델과 위험분담 계약으로 인해 약물 치료 결과가 중요한 성과 지표가 되고 있으며, 의료 시스템과 약국은 부작용과 재입원의 측정 가능한 감소를 입증할 수 있는 솔루션을 개발해야 하는 상황에 직면해 있습니다. 이러한 역학관계에 따라 공급업체와 의료시스템은 확장성, 임상의의 경험, 증거에 기반한 의사결정을 중시하는 플랫폼에 집중하고 있습니다. 이러한 변화로 인해 생태계 전반의 조달 우선순위와 도입 접근 방식이 재편되고 있습니다.

2025년 미국의 관세 동향이 세계 공급망, 조달 비용, 벤더 조달 전략에 미치는 영향에 대한 종합적 분석

2025년 미국의 관세 환경은 처방전 관리 구축과 관련된 하드웨어 조달, 주변기기 조달, 국경 간 공급업체 관계에 영향을 미칠 수 있는 일련의 공급망 고려 사항을 도입할 것입니다. 관세 조정은 디바이스, 서버, 네트워크 장비의 비용 구조에 영향을 미치고, 자본 계획 및 조달 리드 타임에 변동이 발생할 수 있습니다. 그 결과, 이해관계자들은 예측 가능한 배포 일정을 유지하고 총소유비용을 관리하기 위해 벤더의 공급망, 부품 조달, 제조 발자국을 평가해야 합니다.

이에 따라 조달팀은 공급업체의 다양성, 멀티소스 전략, 특정 공급 리스크를 공급업체에 전가하는 계약 조건을 점점 더 중요하게 여기고 있습니다. 이와 함께 공급업체들은 제조 지역화, 대체 유통 채널 활용, 관세로 인한 가격 조정에 대비한 재고 전략 개선 등 적응 방안을 강구하고 있습니다. 이러한 움직임으로 인해 리스크는 줄어들겠지만, 리드타임과 부품 대체 정책에 대한 계약상의 약속을 보다 명확히 할 필요가 있습니다.

또한, 관세에 의한 재조정은 국제적으로 조달된 하드웨어와 타사 서비스에 의존하는 소프트웨어 공급업체에도 영향을 미칩니다. 따라서 처방전 관리 플랫폼을 평가하는 조직은 벤더의 조달 관행, 부품 부족 시 에스컬레이션 프로토콜, 지원 및 유지보수 지속을 위한 컨틴전시 플랜에 대한 투명성을 확보해야 합니다. 이를 종합하면, 2025년 관세 동향은 탄력적인 조달 전략, 계약상 안전장치, 도입 일정 및 임상 연속성을 유지하기 위한 운영상의 유연성, 탄력적인 조달 전략의 필요성을 강조하고 있습니다.

헬스케어 환경에서의 도입 및 ROI를 위한 구성요소, 배포, 최종사용자, 용도, 조직 규모, 심층 세분화 인사이트의 의미를 밝혀줍니다.

세분화에 대한 미묘한 관점을 통해 솔루션 구성요소, 배포 옵션, 최종사용자, 애플리케이션 우선순위, 조직 규모에 따라 솔루션 채택 경로와 가치 실현이 어떻게 달라질 수 있는지를 파악할 수 있습니다. 서비스에는 지원 및 유지보수, 교육 및 컨설팅이 포함되며, 소프트웨어에는 임상 및 운영 기능을 제공하는 핵심 모듈이 포함됩니다. 소프트웨어 중심의 조달은 통합의 용이성과 가동 시간을 우선시하는 반면, 서비스 중심의 계약은 보다 심도 있는 워크플로우 재설계와 지속적인 변경 관리가 필요한 경우가 많기 때문에 이 구분이 중요합니다.

목차

제1장 서문

제2장 조사 방법

제3장 주요 요약

제4장 시장 개요

제5장 시장 인사이트

제6장 미국 관세의 누적 영향 2025

제7장 AI의 누적 영향 2025

제8장 처방 관리 소프트웨어 시장 : 구성요소별

  • 서비스
    • 지원과 유지관리
    • 트레이닝과 컨설팅
  • 소프트웨어

제9장 처방 관리 소프트웨어 시장 : 전개 방식별

  • 클라우드
  • 온프레미스

제10장 처방 관리 소프트웨어 시장 : 최종사용자별

  • 외래 진료 센터
  • 병원과 클리닉
  • 약국

제11장 처방 관리 소프트웨어 시장 : 용도별

  • 임상 의사결정 지원
  • 전자 처방
  • 재고 관리
  • 복약 준수

제12장 처방 관리 소프트웨어 시장 : 조직 규모별

  • 대기업
  • 중소기업

제13장 처방 관리 소프트웨어 시장 : 지역별

  • 아메리카
    • 북미
    • 라틴아메리카
  • 유럽, 중동 및 아프리카
    • 유럽
    • 중동
    • 아프리카
  • 아시아태평양

제14장 처방 관리 소프트웨어 시장 : 그룹별

  • ASEAN
  • GCC
  • EU
  • BRICS
  • G7
  • NATO

제15장 처방 관리 소프트웨어 시장 : 국가별

  • 미국
  • 캐나다
  • 멕시코
  • 브라질
  • 영국
  • 독일
  • 프랑스
  • 러시아
  • 이탈리아
  • 스페인
  • 중국
  • 인도
  • 일본
  • 호주
  • 한국

제16장 경쟁 구도

  • 시장 점유율 분석, 2024
  • FPNV 포지셔닝 매트릭스, 2024
  • 경쟁 분석
    • Epic Systems Corporation
    • Cerner Corporation
    • Allscripts Healthcare Solutions, Inc.
    • Surescripts, LLC
    • McKesson Corporation
    • athenahealth, Inc.
    • eClinicalWorks, LLC
    • Medical Information Technology, Inc.
    • NextGen Healthcare, Inc.
    • DrFirst, Inc.
KSM 25.10.20

The Prescription Management Software Market is projected to grow by USD 4.32 billion at a CAGR of 17.48% by 2032.

KEY MARKET STATISTICS
Base Year [2024] USD 1.19 billion
Estimated Year [2025] USD 1.39 billion
Forecast Year [2032] USD 4.32 billion
CAGR (%) 17.48%

Strategic overview introducing prescription management software value proposition, clinical integration drivers, regulatory pressures, and operational benefits

The prescription management software landscape intersects clinical care, pharmacy operations, and health IT infrastructure in ways that materially affect medication safety, workflow efficiency, and patient experience. This executive summary introduces the core value proposition of prescription management solutions by framing how technology integrates with electronic health records, e-prescribing networks, and pharmacy inventory systems to reduce errors, streamline prescribing workflows, and support adherence interventions. Decision-makers should view these platforms as connective tissue that coordinates clinician intent, pharmacist verification, and patient behavior across distributed care settings.

Moreover, regulatory and reimbursement dynamics increasingly incentivize digital controls and data-driven medication management. As a result, organizations that prioritize interoperability, data governance, and clinician-centric design capture operational benefits more rapidly. In this context, the technology's role extends beyond transaction processing to enable analytics-driven stewardship, targeted patient outreach, and safety surveillance. Consequently, leaders must balance clinical usability with technical robustness, ensuring that deployment strategies mitigate disruption while unlocking measurable improvements in medication outcomes.

Finally, this introduction sets the stage for deeper analysis by emphasizing practical considerations: integration complexity, vendor ecosystem interoperability, change management needs, and the importance of aligning technology choices with clinical pathways. The following sections build on this foundation to explore transformative trends, policy influences, segmentation nuances, regional dynamics, competitive positioning, and actionable steps for implementation.

Transformative forces reshaping prescription management, including AI-enabled decision support, interoperability standards, and patient-centered digital workflows

Prescription management is undergoing transformative shifts driven by advances in artificial intelligence, expanding interoperability frameworks, and a stronger emphasis on patient-centered digital services. AI-enabled clinical decision support now assists clinicians with context-aware prescribing suggestions, formulary-aware alternatives, and automated alerts that prioritize safety while reducing alert fatigue. These capabilities, when paired with real-time data exchange standards and APIs, enable tightly coupled workflows across clinicians, pharmacies, and payers, improving concordance between intent and fulfillment.

At the same time, emerging interoperability standards and certification expectations are reducing integration friction and accelerating data portability. Consequently, organizations can adopt modular approaches that connect e-prescribing engines, inventory controls, and adherence tools without wholesale replacement of legacy systems. Furthermore, the consumerization of health IT-driven by mobile adherence tools, telepharmacy services, and patient portals-creates new touchpoints that extend medication management into the home and community settings.

Equally important, value-based care models and risk-sharing arrangements are elevating medication outcomes as a core performance metric, prompting health systems and pharmacies to deploy solutions that demonstrate measurable reductions in adverse events and readmissions. In light of these dynamics, vendors and health systems are converging on platforms that emphasize extensibility, clinician experience, and evidence-based decisioning. Together, these shifts are reshaping procurement priorities and implementation approaches across the ecosystem.

Comprehensive analysis of how United States tariff dynamics in 2025 influence global supply chains, procurement costs, and vendor sourcing strategies

The tariff environment in the United States during 2025 introduces a set of supply chain considerations that can influence hardware procurement, peripheral sourcing, and cross-border vendor relationships relevant to prescription management deployments. Tariff adjustments affect cost structures for devices, servers, and networking equipment and can introduce variability into capital planning and procurement lead times. As a result, stakeholders must assess vendor supply chains, component sourcing, and manufacturing footprints to maintain predictable rollout schedules and control total cost of ownership.

In response, procurement teams increasingly emphasize supplier diversity, multi-source strategies, and contractual terms that shift certain supply risks to vendors. In parallel, vendors are adapting by regionalizing manufacturing, leveraging alternative distribution channels, and refining inventory strategies to buffer against tariff-driven price adjustments. These moves reduce exposure but require clearer contractual commitments on lead times and component substitution policies.

Moreover, the tariff-driven recalibration extends to software vendors that depend on internationally sourced hardware or third-party services. Organizations evaluating prescription management platforms should therefore require transparency on vendor procurement practices, escalation protocols for component shortages, and contingency plans for sustaining support and maintenance. Taken together, tariff dynamics in 2025 reinforce the need for resilient sourcing strategies, contractual safeguards, and operational flexibility to preserve implementation timelines and clinical continuity.

Deep segmentation insights revealing component, deployment, end-user, application, and organization size implications for adoption and ROI in healthcare settings

A nuanced view of segmentation clarifies how different solution components, deployment choices, end users, application priorities, and organizational scale shape adoption pathways and value realization. Based on Component, offerings divide into Services and Software, where Services encompass support & maintenance and training & consulting, and Software includes core modules that deliver clinical and operational functionality. This distinction matters because services-heavy engagements often require deeper workflow redesign and sustained change management, while software-centric procurements prioritize ease of integration and time-to-live.

Based on Deployment Mode, organizations choose between Cloud and On Premises models, each presenting trade-offs in scalability, data residency, and operational control. Cloud deployments accelerate feature delivery and can streamline vendor-managed updates, whereas on-premises installations maintain local control and can align with strict data governance regimes. Consequently, procurement and IT governance teams must weigh regulatory obligations and operational readiness when selecting a model.

Based on End User, systems are implemented across ambulatory care centers, hospitals & clinics, and pharmacies, each with distinct workflow patterns and stakeholder priorities. Ambulatory care centers favor streamlined e-prescribing and adherence touchpoints, hospitals and clinics require integration with inpatient medication management and clinical decision support, and pharmacies emphasize inventory control and point-of-dispense reconciliation. Based on Application, the focus ranges across clinical decision support, e-prescribing, inventory management, and medication adherence; alignment of feature sets to clinical pathways determines clinician acceptance and downstream outcomes. Finally, based on Organization Size, solutions and procurement approaches differ between large enterprises and SMEs, where large enterprises often require complex integrations and rigorous vendor governance, while SMEs prioritize cost efficiency and rapid deployment. Understanding these segmentation dimensions informs vendor selection, deployment sequencing, and the design of success metrics.

Regional dynamics and strategic considerations across the Americas, Europe Middle East & Africa, and Asia-Pacific shaping technology investment and compliance

Regional dynamics materially influence technology selection, regulatory compliance strategies, and implementation sequencing across major geographies. In the Americas, buyers contend with heterogeneous state-level regulations, robust private payer involvement, and mature e-prescribing networks that emphasize integration with national drug databases. Consequently, vendors active in this region prioritize interoperability with major electronic health record vendors and offer features that facilitate payer reconciliation and formulary alignment.

In Europe, Middle East & Africa the regulatory landscape emphasizes data protection, cross-border privacy considerations, and varying reimbursement mechanisms that require flexible deployment options and strong localization capabilities. Vendors operating here must adapt to multiple languages, regional clinical guidelines, and divergent pharmacy practices, which increases the importance of configurable workflows and local partnership networks. In addition, regulatory authorities in several countries are advancing digital health strategies that incentivize medication safety initiatives, creating fertile ground for targeted deployments.

In Asia-Pacific, rapid adoption of mobile-first patient engagement, expanding telehealth services, and government-led digital health initiatives accelerate demand for scalable cloud solutions. However, fragmentation across national health systems and divergent data localization laws necessitate adaptable architectures and region-specific compliance frameworks. Across all regions, implementation success depends on tailoring change management to local clinical culture, ensuring regulatory alignment, and partnering with local integrators to bridge technical and operational gaps.

Competitive landscape overview of top vendors, partnership approaches, innovation direction, and strategic differentiation in prescription technology

The competitive landscape in prescription management reflects a mix of established health IT vendors, specialized pharmacy systems providers, and emerging platform innovators. Leading vendors differentiate through integrations with major electronic health record platforms, robust clinical decision support capabilities, and proven interfaces to national prescribing and pharmacy networks. Partnership models vary from direct enterprise licensing to ecosystem approaches that bundle third-party services and local implementation partners.

Innovation pipelines emphasize natural language processing for clinician documentation, predictive risk scoring for medication safety, and adherence interventions that blend behavioral science with digital nudges. These initiatives reflect a broader shift toward using data to drive actionable insights at the point of care. Vendors that invest in modular architectures and open APIs increase their appeal to health systems seeking to layer capabilities incrementally while preserving existing investments.

Strategic differentiation also arises from the quality of services: implementation expertise, clinician training programs, and post-deployment support frameworks that reduce operational friction. For many buyers, the ability to demonstrate rapid clinician uptake and reduced medication-related incidents is a decisive procurement criterion. Consequently, competitive advantage resides not only in feature sets but also in evidence of successful rollouts, integration maturity, and the capacity to support long-term operational improvement.

Actionable recommendations for industry leaders to accelerate adoption, optimize integrations, mitigate compliance risks, and deliver measurable clinical outcomes

Industry leaders should adopt a pragmatic, phased approach to accelerate value while minimizing disruption. Begin by aligning clinical leaders, pharmacy stakeholders, and IT governance early in the procurement process to define clinical priorities, data requirements, and integration touchpoints. Establish clear success metrics tied to clinical outcomes and operational efficiency, and ensure governance structures assign accountability for both clinical adoption and technical reliability.

Next, prioritize interoperability and user-centered design in vendor selection. Require demonstrable APIs, certification evidence for standards compliance, and practical usability testing with representative clinician and pharmacy workflows. Simultaneously, negotiate contractual provisions that include service-level commitments for integration support, update cadence, and contingency plans for hardware or component disruptions.

Additionally, invest in structured training and ongoing support to sustain clinician engagement. Tailored training programs that combine role-specific curricula with hands-on simulation reduce adoption friction. Finally, build iterative feedback loops that use implementation data to refine decision support rules, alert thresholds, and adherence interventions. By combining disciplined governance, rigorous vendor selection, prioritized usability, and continuous improvement cycles, leaders can accelerate adoption and realize sustained clinical and operational benefits.

Robust research methodology explaining data sources, primary and secondary research approaches, validation protocols, and analytical frameworks used in the study

This study employs a mixed-methods research design that integrates primary interviews, secondary source synthesis, and qualitative case analysis to ensure evidence-based conclusions and actionable recommendations. Primary research included in-depth interviews with clinician leaders, pharmacy directors, IT architects, and procurement officers to capture real-world deployment experience and priorities. These conversations informed thematic coding that highlighted common barriers and success factors across settings.

Secondary research drew on publicly available regulatory guidance, standards documentation, and vendor technical specifications to validate trends and technical constraints. In addition, select case studies provided longitudinal perspectives on implementation sequencing, change management approaches, and vendor performance. Methodological safeguards included triangulation across data sources, validation workshops with domain experts, and iterative revision to reconcile divergent inputs.

Analytical frameworks combined capability mapping, stakeholder impact analysis, and readiness assessments to produce pragmatic guidance for decision-makers. The research team applied sensitivity checks to ensure recommendations remain useful across deployment models and organizational scales. Where appropriate, the study flags areas that require localized validation, such as regulatory interpretations and integration specifics, and recommends targeted pilots to de-risk broader rollouts.

Concluding insights synthesizing implications for providers, payers, vendors, and policymakers to inform strategic priorities and next steps in implementation

This executive summary synthesizes the study's implications for providers, payers, vendors, and policymakers and outlines pragmatic next steps. For providers, the imperative is to prioritize clinician-centered integration and to align procurement with interoperability and change management capacity. Payers should evaluate how medication management technologies can be incorporated into value-based arrangements and quality programs that reward improved medication outcomes.

Vendors must continue to invest in modular architectures, open APIs, and evidence-generation to demonstrate clinical impact. Partnerships with local integrators and clinical champions will accelerate deployment and uptake. Policymakers play a role by clarifying data governance expectations, promoting standards that reduce integration complexity, and supporting initiatives that incentivize safe prescribing practices.

Looking forward, organizations that combine technical rigor with disciplined implementation governance will unlock the greatest benefits. By piloting targeted interventions, measuring outcomes, and scaling iteratively, stakeholders can reduce risk while delivering demonstrable improvements in medication safety and operational efficiency. These conclusions provide a pragmatic foundation for action and a roadmap for translating insight into sustained performance improvement.

Table of Contents

1. Preface

  • 1.1. Objectives of the Study
  • 1.2. Market Segmentation & Coverage
  • 1.3. Years Considered for the Study
  • 1.4. Currency & Pricing
  • 1.5. Language
  • 1.6. Stakeholders

2. Research Methodology

3. Executive Summary

4. Market Overview

5. Market Insights

  • 5.1. Integration of AI-powered predictive analytics into prescription management for proactive adherence interventions
  • 5.2. Seamless interoperability between EHR systems and e-prescribing platforms via FHIR-based APIs
  • 5.3. Real-time prescription benefit verification integrated at point of care to lower patient out-of-pocket costs
  • 5.4. Blockchain-enabled secure prescription transmission networks reducing fraud and enhancing data integrity
  • 5.5. Integration of telehealth services with digital prescription management to streamline virtual patient care workflows

6. Cumulative Impact of United States Tariffs 2025

7. Cumulative Impact of Artificial Intelligence 2025

8. Prescription Management Software Market, by Component

  • 8.1. Services
    • 8.1.1. Support & Maintenance
    • 8.1.2. Training & Consulting
  • 8.2. Software

9. Prescription Management Software Market, by Deployment Mode

  • 9.1. Cloud
  • 9.2. On Premises

10. Prescription Management Software Market, by End User

  • 10.1. Ambulatory Care Centers
  • 10.2. Hospitals & Clinics
  • 10.3. Pharmacies

11. Prescription Management Software Market, by Application

  • 11.1. Clinical Decision Support
  • 11.2. E-Prescribing
  • 11.3. Inventory Management
  • 11.4. Medication Adherence

12. Prescription Management Software Market, by Organization Size

  • 12.1. Large Enterprises
  • 12.2. SMEs

13. Prescription Management Software Market, by Region

  • 13.1. Americas
    • 13.1.1. North America
    • 13.1.2. Latin America
  • 13.2. Europe, Middle East & Africa
    • 13.2.1. Europe
    • 13.2.2. Middle East
    • 13.2.3. Africa
  • 13.3. Asia-Pacific

14. Prescription Management Software Market, by Group

  • 14.1. ASEAN
  • 14.2. GCC
  • 14.3. European Union
  • 14.4. BRICS
  • 14.5. G7
  • 14.6. NATO

15. Prescription Management Software Market, by Country

  • 15.1. United States
  • 15.2. Canada
  • 15.3. Mexico
  • 15.4. Brazil
  • 15.5. United Kingdom
  • 15.6. Germany
  • 15.7. France
  • 15.8. Russia
  • 15.9. Italy
  • 15.10. Spain
  • 15.11. China
  • 15.12. India
  • 15.13. Japan
  • 15.14. Australia
  • 15.15. South Korea

16. Competitive Landscape

  • 16.1. Market Share Analysis, 2024
  • 16.2. FPNV Positioning Matrix, 2024
  • 16.3. Competitive Analysis
    • 16.3.1. Epic Systems Corporation
    • 16.3.2. Cerner Corporation
    • 16.3.3. Allscripts Healthcare Solutions, Inc.
    • 16.3.4. Surescripts, LLC
    • 16.3.5. McKesson Corporation
    • 16.3.6. athenahealth, Inc.
    • 16.3.7. eClinicalWorks, LLC
    • 16.3.8. Medical Information Technology, Inc.
    • 16.3.9. NextGen Healthcare, Inc.
    • 16.3.10. DrFirst, Inc.
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