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 trainingthat closes gaps, aligns daily work with regulatory standards, and holds up under inspection.
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)
Our course provides a comprehensive roadmap for successful adoption of E6(R3), enabling organizations to minimize compliance risks, optimize operational efficiency.
We develop protocol-specific training programs that help sites navigate those requirements through structured, interactive formats designed for clinical workflows.
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
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.