Clinical reporting

The TCC employs academically qualified medical writers who are experienced in addressing all requirements for reporting clinical studies. The structure and content of our clinical study reports conform to appropriate legal requirements. For example, we use the regulations for reporting on clinical trials laid down by the International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use (ICH). We also use these guidelines when preparing clinical study reports for other types of clinical research.

The results of all studies are reported to the sponsors, ethics committees and competent authorities. Also, results of a study may be presented at conferences or in scientific journals. Our staff can then help ensure that the study and analysis have been properly described and the results correctly interpreted. If required, we can also provide additional statistical consultancy and writing support to help you disseminate your results across the scientific community.