CPR is your premier CRO for early Phase monitoring but provides expertise in monitoring across all phases of clinical trials having had significant experience in managing the Australian arm of multi-national Phase III trials.  

 CPR Pharma 2016

All trials are monitored in accordance with Australian regulatory requirements and ICH GCP. Our CRAs undergo targeted internal and external training to compliment their extensive experience in early phase monitoring.

To ensure the seamless exchange of information each project is assigned a manager as a single point of contact.

CPRs Quality Assurance department audits and reports on the monitoring, collection and  reporting of accurate, precise, and valid data.

CPR has an extensive Suite of Standard operating procedures to conduct clinical trial activities. Additionally  CPR can adapt seamlessly to your SOP’s and requirements if desired.

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