Our Services
We can help you with advice on:
- Trial design
- Implementation Research (helping translation into clinical practice)
- Outcome measures, including Quality of Life and other patient-reported outcomes (PROs)
- Quality assurance and monitoring processes
- Biostatistics
- Health economics
And by:
- Conducting background research, including systematic reviews
- Coordinating meetings and teleconferences for investigators
- Assisting with ethics and regulatory applications
- Brokering collaborations
- Developing patient recruitment materials
To become a PC4 supported trial, researchers provide evidence of ethics approval and appropriate trial registration, provide six-monthly reports to the PC4 Office and acknowledge PC4 support in all reports, publications and presentations.
Biostatistics
Our biostatistics support can help inform your trial design, conduct and analysis including:
- Protocol development and review
- Sample size and power calculations
- Determining appropriate analytical methods
- Determining appropriate randomisation schemes
- Correct data interpretation methods
- Assistance selecting data management systems
- Statistical modelling
Clinical Trial Registration
PC4 can assist you in registering your research with the most appropriate clinical trial registry. Online registries of clinical trials have been established for a wide range of research, and have many purposes. Some aim to inform researchers of like-minded colleagues and their work, others encourage patients to enquire about the potential for participation. Many consumer organisations promote participation in clinical trials because there is some evidence that indicates such patients receive the best clinical management.