For example, requesting a description of the study design in line with the guidelines in funding or ethical review applications ensures that steps to minimise experimental bias are considered at the beginning of the research cycle (Updated RCUK guidance for funding applications involving animal research...
In addition, 12 months after finalization of the clinical trial, a summary of the trial's results and a layman's summary, both prepared by the sponsor of the trial, will be made available through CTIS. CTIS will also include the clinical study reports (CSRs) for clinical trials conducted...