JMP® Clinical: Generating Semi-Automated Patient Narratives for Regulatory Submissions
Oct. 14, 2021 | 2:00 p.m. ET
This session is for JMP Clinical users interested in learning to efficiently and accurately generate patient narratives and patient profiles. See how to generate documents to accompany Clinical Study Reports (Regulatory Submission document) for Serious Adverse Events, Permanently Discontinued Subjects Reports, Adverse Events of Special Interest Reports, and reports on Adverse Events associated with Specific Standard MedDRA Queries (Medical Dictionary for Regulatory Activities disease associated adverse events).