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      • HOME
      • WHY PRISMS
      • SERVICES
      • PORTFOLIO
      • MISSION
      • BLOG
      • LOCATIONS
      • CONTACT US

    ​

      • HOME
      • WHY PRISMS
      • SERVICES
      • PORTFOLIO
      • MISSION
      • BLOG
      • LOCATIONS
      • CONTACT US
      • …  
        • HOME
        • WHY PRISMS
        • SERVICES
        • PORTFOLIO
        • MISSION
        • BLOG
        • LOCATIONS
        • CONTACT US

      ​

      • OUR SERVICES

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        HOSPITAL SYSTEMS AND CLINICS

        • Synergistic Approach: Facilitate a symbiotic partnership between Physician Investigators and Pharmaceutical Sponsors
        • Patient Community: Empower your patients to enhance their overall lives, extending the impact of healthcare beyond treatment and fostering a sense of well-being
        • Growth Advance: Additional source of physician referral, academic breadth, and marketing
        • Financial Advantages: Optimize leverage and execution of favorable revenue fees
        • Recognized Gains: Assertively manage trial patient billing
        • Deliverables: Punctual execution and adept trial management ensure regulatory compliance and strategically yield cost savings
        • Strategic ROI: Diminish operating costs associated with site-level research activities

        BIOPHARMA INDUSTRY

        • Exclusive Multi-Site Network: Access top investigators across multiple sites for widespread trial impact.
        • Rapid Study Start-Up: Streamlined initiation ensures minimal delays and faster study commencement.
        • Precise Data Delivery: Punctual, accurate data empowers informed decision-making.
        • High Patient Accrual: Accelerated recruitment from a diverse participant pool.
        • Prequalified Site Efficiency: Expedite studies with prequalified sites, reducing administrative burdens.
        • Integrated Technology Tools: Seamlessly integrate cutting-edge tools for enhanced data management.
        • Patient Matching Database: Access a comprehensive network-wide database for targeted participant identification.
        • On-Site Professional Staffing: Ensure optimal study execution with dedicated on-site professionals.

        GROWTH & REVENUE

        • Seamless and Proficient Management of Trial Patient Billing Processes
        • Punctual Execution and Strategic Trial Management Resulting in Significant Cost Savings for Clients
        • Substantial Reduction of Operational Costs Through Efficient Management of Research Activities at the Site Level
        • Implementation of Advanced Financial Strategies for Budgetary Optimization
        • Continuous Evaluation and Adaptation of Financial Strategies for Ongoing Operational Excellence

        QUALITY & DELIVERABLES

        • Investigators and site selection based on clinical expertise and adherence to ICH Good Clinical Practice (GCP) and FDA CFR guidelines.
        • Robust internal audit process ensuring high-quality data.
        • Rigorous Monitoring and Oversight Ensuring Fiscal Efficiency Throughout the Trial Lifecycle
        • Stringent data integrity oversight, influencing repeat site selection.
        • Streamlined processes for investigators, alleviating staff burden and facilitating optimal trial performance.
      • OUR PORTFOLIO

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        HELP SOLVE DISEASES
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        LUNG CANCER
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        BREAST CANCER
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        COVID-19 STUDY
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        CHRONIC HEART FAILURE TRIAL
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        GALL BLADDER CANCER TRIAL
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        ADVANCED CANCER
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        COVID PLASMA TRIAL
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        LYMPHOMA
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        COLON CANCER
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        PROSTATE CANCER
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        HEPATITIS STUDY

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