At Confidence, we pride ourselves on adhering to the highest standards of scientific research.
Our Clinical Data Management and Statistics team are involved in project planning from the outset, collaborating closely with other functional groups and contributing to key study decisions.
Our Biostatisticians are seasoned veterans of the clinical trial process, involved in every step of the way – from developing the Statistics section of the protocol, to engaging with regulatory bodies like the FDA and other Competent Authorities, to creating the Statistical Programming Plan and Statistical analysis, and finally producing the Clinical Study Reports.
Our programmers and Data Management specialists have extensive experience working with a variety of EDC systems, and can work with your chosen solution or propose our own.
- Creating the Data Management Plan
- Developing the electronic Case Report Form (eCRF)
- Building and validating the Electronic Data Capture (EDC) system
- Providing the final Database Lock