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    • Home
    • Clinical Operations
    • Clinical Data Management
    • Biostatistics
    • Medical Writing
    • Regulatory Services
    • Quality Assurance
    • Preclinical Data Services
    • Clinical Services
  • Home
  • Clinical Operations
  • Clinical Data Management
  • Biostatistics
  • Medical Writing
  • Regulatory Services
  • Quality Assurance
  • Preclinical Data Services
  • Clinical Services

Clinical Services

 

Real World Evidence (RWE) and Healthcare Research Services


We deliver end-to-end Real World Evidence (RWE) and healthcare research solutions that generate actionable insights to support clinical development, regulatory submissions, market access, and patient outcomes. Our RWE and healthcare research services include:


  • Real World Data (RWD) strategy and study design
  • Observational and non-interventional studies
  • Registry design and management
  • Claims, EMR, and EHR data analytics
  • Health Economics and Outcomes Research (HEOR)
  • Patient-reported outcomes (PROs) and digital health studies


Leveraging advanced analytics, AI-driven insights, and robust data governance frameworks, we transform complex real-world data into credible evidence. Our solutions are designed to meet evolving regulatory expectations while supporting value demonstration across the product lifecycle.


Functional Service Provider (FSP) Services


We deliver Functional Service Provider (FSP) services that provide sponsors and CRO partners with embedded, high-performing clinical research capabilities across the development lifecycle. Our FSP model is designed to offer flexibility, operational excellence, and seamless integration with your internal teams—while maintaining the highest standards of quality and compliance.

Under our FSP engagement model, our experts operate as an extension of your organization, supported by standardized processes, technology-enabled workflows, and robust governance frameworks. This ensures predictable delivery, scalability, and continuity across programs and portfolios. Our FSP Capabilities Include:


  • Clinical Research Associates (CRAs)
  • Clinical Project & Program Managers
  • Clinical Data Managers
  • Biostatisticians & Statistical Programmers
  • Medical Writers
  • Pharmacovigilance & Safety Experts
  • Regulatory Affairs Specialists


Our FSP teams are enabled by digital onboarding, centralized training, performance analytics, and quality oversight to ensure alignment with global regulatory requirements, including ICH-GCP, FDA, EMA, and regional regulations. We offer both role-based and functional ownership models, tailored to meet evolving program demands.


By combining domain expertise with technology and data-driven delivery, our FSP services help reduce operational complexity, improve efficiency, and accelerate clinical development—without compromising scientific rigor or compliance.

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