GCP Central is provider of online training in regulations that impact clinical research, including Good Clinical Practices (ICH-GCP), Clinical Trials Regulation (EU CTR), WMO, Medical Device regulation (MDR) and GMP. 

We provide trainings to both clinical research sites, CROs, and sponsors. Our modern approach to training directly impacts the quality of clinical research and compliance to guidelines and regulations. Increasing the data quality, integrity and transparency in sponsor systems and supporting audit readiness.

It is our goal to make sure clinical research professionals are knowledgeable about guidelines and regulations through effective tools, highly interactive training and pioneering new learning methods on a global scale.

We put GCP knowledge at the fingertips of sponsors, CROs, investigators and site staff and make it a core part of their everyday practice.