At The QARP, our consultants and trainers are senior GCP auditors.
We’ve seen what fails in practice and we built our approach to fix it: one integrated system of auditing, consulting, and training that closes gaps, aligns daily work with regulatory standards, and holds up under inspection.

This is about us:

  • 20 +
    years of experience in the international clinical trials market
  • 1400 +
    prepared and delivered trainings and workshops in Clinical Trial area
  • 1000 +
    Audits delivered across 5 continents

Latest updates:

    The QARP Experts Published in RQA’s Journal
    Our article “Beyond Box Ticking” explores how adaptive, AI-driven training improves compliance and quality in clinical trials now published in Quasar #172 (August 2025)

    They trust us:

    Our Audits

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    Our Academy

    • Our course provides a comprehensive roadmap for successful adoption of E6(R3), enabling organizations to minimize compliance risks, optimize operational efficiency.

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    • We develop protocol-specific training programs that help sites navigate those requirements through structured, interactive formats designed for clinical workflows.

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    • A compact, expert-led format for organizations that use internal materials to onboard staff on E6(R3).
      If your staff has already been trained in-house, this solution closes the remaining gap
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    • This course is grounded in global standards, including GAMP® 5, GMP Annex 11, and CFR Title 21 Part 11, and is essential for professionals involved in the implementation and validation of computerized systems.
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    Our Сonsulting

    • Structured, Unbiased Oversight Supporting Inspection Readiness and Trial Quality
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    • Structured support for aligning with updated GCP standards
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    • A compact, expert-led format for organizations that use internal materials to onboard staff on E6(R3).
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    CONTACT US

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