The dynamic development of the area of clinical studies in Poland and worldwide has led us to a particularly extensive experience in this field. We support all the actors involved in the research project – from CROs and research sponsors to clinical centres or medical facilities. We are equipped with both linguistic proficiency and expertise in specialist vocabulary, as well as a good command of documentation created for the purposes of research processes. So you can entrust us with translation of materials from any stage of a clinical study — from requesting the initiation of the study and recruitment of patients to the final results and marketing of the medicinal product.
Verifying the safety of medicinal products and their effects on the body is an extremely long procedure. The clinical trial documentation submitted to us for specialist translation can be divided into two parts. The first one is created before the start of a specific phase of the planned research. The second one is created after the research is finished. Such documents include forms, minutes, summaries, summaries, leaflets, posters or official correspondence. In addition, clinical studies of new drugs or products are subject to many regulations regulated by EU laws and directives.