Careful planning is the key
Statistical analysis of a clinical trial is more complex than completing a couple of t-tests in Microsoft Excel and most ethics committees know this! Careful consideration of the proposed analysis at the time of designing the trial is crucial. Whether you are considering a large randomized clinical study to underpin product registration or providing support for a small investigator-initiated trial. We will work with you to determine appropriate analyses for your study and assist in the preparation of the statistical section of the protocol and to ensure that the objectives of the study can be achieved.