The QARP
GxP Experts:
Auditing. Consulting. Training.
GxP Experts:
Auditing. Consulting. Training.
Promo Code “Winter25”: this is our winter offer.
Winter pricing for all services
December 1–31, 2025: 25% off training, audits, and consulting.
The rate applies to the full service portfolio to support team preparation, regulatory tasks, and process work while controlling budget impact.
Submit a request to receive the winter price for your projects or use promo code “Winter25”.
The rate applies to the full service portfolio to support team preparation, regulatory tasks, and process work while controlling budget impact.
Submit a request to receive the winter price for your projects or use promo code “Winter25”.
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 Academy
- 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.
Our Сonsulting
- Structured support for aligning with updated GCP standards
- A compact, expert-led format for organizations that use internal materials to onboard staff on E6(R3).