CPR monitors are specifically trained and have extensive experience with early phase monitoring. CPR also offers monitoring across all clinical trial phases with experience in managing the Australian arm of multinational Phase III trials. All trials are monitored in accordance with ICH GCP.

CPR is commited to achieving high standards of professional and ethical conduct as well as validity and accuracy in the collection and reporting of data. To ensure the highest standards of quality and consistency during monitoring are met our QA performs regular co-monitoring and ongoing training for all monitors. We provide the flexibility of working to CPR SOPs or will quickly adapt to your SOPs and requirements.