Clinical Summaries present a comprehensive and factual summarisation of all the clinical information in the Common Technical Document (CTD). Each summary focuses on a specific area and, taken together, they help regulatory authorities to assess how the medicine works, how it is absorbed, how safe it is, and its effectiveness in patients. Therefore, drafting these documents involves synthesizing large amounts of data into focused deliverables. It is paramount for us to provide documents of the highest standard that fully meet these requirements, while maintaining the accuracy of results and consistency across sections.