Menu
Supporting Clinical Investigational Sites, Sponsors, Contract Research Organizations (CROs), and Clinical Research Educational Organizations in implementing a First Time Quality culture and enhancing Good Clinical Practice (GCP) compliance.
GCPre Consulting is a small independent consultancy that provides dedicated and customer-adapted clinical research services tailored to meet the unique and evolving requirements of the clinical research industry.
We specialize in providing custom-made support to clinical research sites, pharmaceutical and biotechnology companies, CROs, and clinical research educational organizations in their clinical research activities.
Whether you are a big pharmaceutical company or a small biotechnology firm, we can ease your drug development journey by supporting you during the clinical phases and guiding you in meeting your Good Clinical Practice (GCP) responsibilities as a Sponsor.
Whether a naïve research site or an experienced research clinic, we can prepare your site and your staff to implement Good Clinical Practice (GCP) at all stages of the clinical trial. We offer both standalone trainings and continuous support on GCP and its implementation. We can perform a GCP risk assessment of your site and coach you on best practices and regulatory standards, ensuring that your team is always prepared and compliant.
© 2024 GCPre Consulting. All rights reserved
Marisol Diaz
+49 176 8007 8064
contact@gcpreconsulting.com