Global Real World Evidence Solutions Market

Real World Evidence Solutions Market Size, Share, Growth Analysis, By Component(Services, and Data Sets), By Application(Drug Development & Approvals, Medical Device Development & Approvals, Post-Market Surveillance, Market Access & Reimbursement/Coverage Decision-Making), By Deployment Mode(On-Premise Deployment Model, and Cloud-Based Deployment Model), By Revenue Model(Pay Per Use (Value-Based Pricing), and Subscription), By End User(Pharmaceutical & Medical Device Companies, Healthcare Payers, Healthcare Providers, and Other End Users), By Region - Industry Forecast 2024-2031


Report ID: SQMIG35I2180 | Region: Global | Published Date: September, 2024
Pages: 242 | Tables: 90 | Figures: 76

Real World Evidence Solutions Market Dynamics

Real World Evidence Solutions Market Driver

Adoption of AI  

  • AI will enable pharmaceutical and biotech companies to increase meaningful real-world evidence output, substantially reduce the time required to derive valuable insights, and leverage all available data sources. AI-driven analytics and automation help access vital insights contained in historical clinical trial data, as well as real-world data and real-world evidence, thereby expanding the end-to-end clinical trial capabilities.  

Growing Use of Big Data in Healthcare Industry 

  • Advancements in data management and integration have facilitated the speed & quality of drug discovery and clinical trials as well as data use in pharma and biotech companies. Big Data improves real-world data by enhancing anomaly detection, standardization, and quality checking during pre-processing. The RWE platforms will benefit from the use of Big Data and advanced data processing and analysis techniques.  

Restraints 

Limited Skilled Professionals  

  • The main factor which inhibits positive dynamics in the market of real-world evidence solutions is the absence of professionals capable of working with new digital solutions. The gap between the available and required professional workforce in the industry that is engaged in clinical research is impeding the acquisition and utilization of complex, advanced, and hard digital solutions in the sphere of clinical trials.  

Lack of Standardization 

  • One of the considerable threats to market growth is the lack of standardization regarding regulatory, legal, and ethical requirements. Specifically, with reference to analytics concerning real-world data and real-world evidence, the lack of standardization can result in the analysis of the inferior quality, lack of transparency in terms of techniques used, inability to incorporate data provided by different sources and poor reliability of results. 
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FAQs

Global Real-World Evidence Solutions Market size was valued at USD 1.54 billion in 2022 and is poised to grow from USD 1.80 billion in 2023 to USD 6.26 billion by 2031, growing at a CAGR of 16.9% in the forecast period (2024-2031).

The industry is characterized by high innovation levels. The increasing usage of the AI & ML and growing interest in digital health solutions and IT solutions drive the industry. To expand the current market position, the major corporations in the market are increasing their investments in research and development to finance the creation of strategically new products and the acquisition of timely technological advances. Moreover, governmental funding, technological advances, regulatory approvals, changing product portfolios and mergers and acquisitions have been just as vital. It is expected that the major players will leverage the momentum of new product launches during the forecast period, as well as further expand their operations to support their existing lead on the global market for Real World Evidence Solutions.  'IQVIA Holdings Inc. (US) ', 'Merative (US) ', 'Optum, Inc. (US) ', 'ICON PLC (Ireland) ', 'Syneos Health, Inc. (US) ', 'Parexel International Corporation (US) ', 'Thermo Fisher Scientific Inc. (US) ', 'Fortrea Inc. (US) ', 'Oracle Corporation (US) ', 'Elevance Health, Inc. (US) ', 'SAS Institute Inc. (US) ', 'Aetion, Inc. (US) ', 'TriNetX LLC (US) ', 'Trinity (US) ', 'PerkinElmer Inc. (US) ', 'Cognizant Technology Solutions Corporation (US) ', 'Cegedim Health Data (France) ', 'Verantos (US) ', 'Medpace Holdings, Inc. (US) ', 'HealthVerity, Inc. (US) ', 'Datavant (US) ', 'Syapse, Inc. (US) ', 'Tempus (US) ', 'Flatiron Health (US) ', 'Quantzig (UK)'

AI will enable pharmaceutical and biotech companies to increase meaningful real-world evidence output, substantially reduce the time required to derive valuable insights, and leverage all available data sources. AI-driven analytics and automation help access vital insights contained in historical clinical trial data, as well as real-world data and real-world evidence, thereby expanding the end-to-end clinical trial capabilities.  

Increasing Demand for End-to-End Services: An end-to-end approach to utilizing a life sciences company’s data, evidence, and knowledge assets allows making insight-driven decisions from the R&D phase up to commercialization. To seize the opportunities that come with RWD and RWE, various stakeholders provide end-to-end and late-phase services for their clients, including study planning, development of study protocols, study management and reporting, as well as a range of other services.  

North America dominated the market in 2023. The rising demand for real world evidence solutions in North America is primarily supported by significant support from regulatory bodies for using RWE solutions. Further, the shift from volume to value-based care and an increase in R&D spending are anticipated to support market growth. The real-world evidence solutions market in the U.S. is majorly driven by the increasing number of payers using RWD, favorable regulatory environment, increasing number of players providing RWE services, and increasing number of biopharmaceutical companies that are adopting RWE solutions for the approval of their drugs.  

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Global Real World Evidence Solutions Market

Report ID: SQMIG35I2180

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