A regulаtоry аffаirs specialist is preparing the clinical sectiоns оf Module 2 of a CTD dossier. The following content is proposed:1. Inclusion of full clinical study reports and individual patient data listings. 2. A critical, interpretive overview of clinical efficacy and safety, including benefit–risk evaluation and relevance to clinical practice. 3. Integrated, structured summaries of clinical efficacy and safety across studies, including pooled analyses where appropriate. 4. Tabulated presentations of key clinical study results to support the summaries.