CPR is recognised for its high quality research outcomes in collaboration with the pharmaceutical and biotechnology industry. We develop strong working relationships with our clients and provide a customised, project-orientated approach to meet their needs.

CPR believes that irrespective of how complex a project is, the client should always be fully informed of the project’s status. Our team is highly responsive and is readily able to access specialist consultants (pharmacokinetic, analytical, medical, statistical) if required.

We pride ourselves on achieving short lead-times by selecting an optimally resourced team to suit your project needs. All projects are assigned to a project manager who ensure that milestones are reached and timelines are met within the budget.

Our project managers and monitors are involved in all aspects of clinical trial management, including:

• Feasibility assessments
• Study design
• Protocol review / Protocol development
• Development of patient information and consent forms
• HREC submissions
• Case report form design and development
• Investigator selection / Facilitating investigator meetings
• Site selection
• Pre-study visits
• Initiation visits
• Monitoring
• Close-out visits
• Report writing
• Archiving