GCPre Consulting for Clinical Sites

GCP Training for Investigators and Clinical Site staff

GCP training is essential for maintaining high standards in clinical research, ensuring that trials are conducted ethically, and in compliance with regulatory requirements.

We train Investigators and Site staff with our engaging and effective ICH-GCP training, designed to truly educate clinical research professionals rather than just ticking a box. Our training is available as both full and refresher courses, delivered live, either in person or remotely, offering flexibility to suit your needs.

Additionally, we offer tailored GCP trainings focusing on particular GCP topics to cater to your specific needs.

GCP Risk Assessment

Our extensive experience working with clinical research sites from different perspectives has given us the understanding of the main areas where clinical sites face more GCP challenges. We use this knowledge to offer a unique GCP risk assessment that helps the clinical sites appropriately address GCP risks before they become a problem.

The comprehensive nature of our risk assessment ensures the applicability of the results to all clinical trials conducted at the site (ongoing and future) and contributes to increasing the chances of being selected for new clinical trials and to the reduction in the number and severity of audit and inspection findings.

GCP Consultancy

Integrating GCP compliant practices into a clinical site’s processes can be challenging. At GCPre Consulting we can help you harmonize your processes and standard practices across clinical trials to reduce bias, inconsistencies and increase GCP compliance.

We offer remote GCP consultancy adapted to your needs, as one-time or regular communications, via email or phone, adapting to your preferred method of communication.