Services 3C (Clinical Competence Centre)
Our team provides expert support in project management, clinical trial documentation, statistics and clinical data management, simplifying your research process while maintaining the highest standards.
- Please note that our role is to provide advice and support to improve your research, not to conduct the research itself.
Biomedical statistics
Biomedical statistics
Consultancy on: comprehensive statistical analysis to ensure the quality and success of clinical trials. Our services cover a wide range of statistical methods, from study design to predictive modelling, tailored to your specific research needs.
- Comprehensive statistical consulting
- Study design and sample size calculation
- Data analysis and interpretation
- Advanced predictive modelling and machine learning methods
Ticket: Statistical Support Request
Clinical trial documentation
Clinical trial documentation
Advice on: accurate and thorough documentation that is critical for clinical trials. Our services include the preparation of essential documents and the management of risk and regulatory submissions.
- Clinical trial plans
- Risk management reports and guidelines
- Ethics and regulatory submission guidelines
Clinical data management
Clinical data management
Consultancy on: essential data management services for successful clinical trials. These include data checks, data preparation, standardised data collection, early sponsor involvement, eCRF planning and validation and expert advice.
- Data management plan and review
- CRF design and development
- Data entry and documentation
Ticket: Clinical Data Management Support
Project management
Project management
Advice on: Optimising research projects through comprehensive project management and resource allocation and empowering scientists to turn their ideas into impactful research.
- Research design and resources
- Compliance and regulations
- Reporting and knowledge sharing
Ticket: Ongoing Project Support