Advanced GCP in Action: Real-world Insights from Audits & Inspections GCP on October 01-02, 2026 in Bratislava, Slovakia

This advanced training program is designed to deliver practical, real-world insights into Good Clinical Practice (GCP), with a strong emphasis on audits and regulatory inspections in clinical trials. It provides a comprehensive understanding of compliance requirements, focusing on key areas such as data integrity, risk identification, and adherence to global regulatory standards including ICH-GCP guidelines.

Participants will explore common audit findings, inspection trends, and frequent compliance challenges faced across the clinical research landscape. The program highlights effective strategies for audit readiness, including preparation techniques, documentation practices, and approaches to managing inspection outcomes. Through scenario-based learning and case studies, attendees will develop critical thinking skills and gain the ability to apply GCP principles in real-world situations.

Led by an experienced GCP expert with regulatory insight, the training offers valuable perspectives drawn from practical audit and inspection experience. It is designed for professionals in clinical research, quality assurance, and regulatory affairs who aim to strengthen their compliance knowledge, enhance quality systems, and confidently manage audits and inspections while ensuring patient safety and data reliability.