Clinical Laboratory Improvement Amendments (CLIA)

Pro-QCP is designed to simplify and enhance compliance with CLIA standards. It implements a robust Continuous Quality Improvement (CQI) process tailored to your lab’s unique needs, identifying additional process controls that reduce errors and ensure accuracy.

Here’s How it Works

Pro-QCP will guide you step-by-step through a comprehensive risk assessment of your entire diagnostic test process – specific to your particular test method and unique environment – to identify and address your lab’s potential sources of error, to facilitate a continuous quality improvement process, and to generate an inspection-ready Individualized Quality Control Plan (IQCP).

Pro-QCP will also help ensure regulatory compliance and allow you to standardize QA procedures across a variety of test platforms and testing locations:

  • Identify and prioritize potential sources of error in your test process (risks)
  • Inventory everything you are currently doing to prevent those errors (QCP’s)
  • Suggest initiatives and opportunities to further reduce errors
  • Helps determine appropriate external Quality Control frequency in the context of your comprehensive quality control plan
  • Evaluate and approve any remaining residual risk
  • Document all of the above into a federally-compliant IQCP
  • Pro-QCP will also help ensure regulatory compliance and allow you to standardizev QA proPro-QCP allows you to incorporate your historical performance data into your risk assessment, capture citations to federal and accreditation organization requirements, and embed links within your IQCP to your lab’s specific policies and procedures.

    In addition to a comprehensive IQCP, Pro-QCP will generate a Suggestion Report. This report is for internal use and is the basis for a continuous quality improvement program, allowing you to identify and prioritize actions and initiatives that will further mitigate errors over time.

    Pro-QCP is a learning program and over time will incorporate new QCP’s that have been field-tested by our community of users. These additions may represent innovative or creative new quality assurance measures or simply proven best practices. When you return to Pro-QCP over time, you should expect to see new QCP suggestions and further opportunities to reduce errors in your lab.

    Pro-QCP comes pre-populated with references to your lab’s specific regulatory and accreditation requirements, as well as to the specifications for your particular test platform.

    See first hand how Pro-QCP can improve the accuracy of your lab’s test results, drive efficiencies and economies, improve the outcomes of your patients, and help ensure satisfactory regulatory compliance:

    Your First Module is Free
    No Credit Required

    • Choose a Pro-QCP module to trial
    • Log in and see how Pro-QCP can improveyour patient outcomes
    • Enter the code “IQCP-UPGRADE” at checkout

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    The Clinical Laboratory Improvement Amendments (CLIA) have long set the benchmark for quality and accuracy in laboratory testing across the United States. With Pro-QCP™ delivering solutions to meet CLIA standard, CarePoint has an unmatched opportunity to redefine lab efficiency and quality management in a rapidly growing market.

    By automating and enhancing Continuous Quality Improvement (CQI) processes, Pro-QCP™ identifies and implements additional process controls that reduce errors, optimize workflows, and ensure testing accuracy. As labs face increasing regulatory scrutiny, Pro-QCP™ emerges as a game-changing solution, empowering labs to not only meet but exceed CLIA standards while driving measurable improvements in performance and reliability.

    Our flagship product, Pro-QCP™, is a first-to-market SaaS quality management solution designed to help laboratories meet CLIA standards with ease.

    Simplified CLIA Compliance

    Error Reduction and Risk Mitigation

    Enhanced Continuous Quality Improvement (CQI)

    Optimized Workflow Efficiency

    Improved Test Accuracy and Reliability

    Proactive Performance Monitoring