{"id":1322,"date":"2026-08-10T07:48:35","date_gmt":"2026-08-10T07:48:35","guid":{"rendered":"https:\/\/nokobox.com\/index.php\/item\/jmp-clinical-18-0-x64\/"},"modified":"2026-08-10T07:48:35","modified_gmt":"2026-08-10T07:48:35","slug":"jmp-clinical-18-0-x64","status":"publish","type":"digital_item","link":"https:\/\/nokobox.com\/index.php\/item\/jmp-clinical-18-0-x64\/","title":{"rendered":"JMP Clinical 18.0 x64"},"content":{"rendered":"
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Description<\/span><\/h2>\n

JMP Clinical offers tools to make it easy for key participants in the trial review process to explore trends and outliers, detect hidden data, identify safety and efficacy issues, and perform medical monitoring, data integrity validation, and statistical analyses. Summary dashboards in JMP Clinical enable medical reviewers to evaluate safety and efficacy issues with the click of a button. Create interactive reports of adverse events, concomitant medications, labs, and vital signs; drill down to customized patient profiles and patient narratives. Producing adverse event narratives for clinical study reports (CSRs) can be a painstaking, time-consuming process with significant consequences for inaccuracies or delays. With JMP Clinical, medical writers can automate patient profiles and patient narratives to reduce the time and complexity of creating output for review and submission to regulatory agencies. The goal of clinical operations is to mitigate data quality risks that could hinder a regulatory submission or drug approval. Risk-based monitoring tools in JMP Clinical help you identify data anomalies at the vendor, monitor, site, and country level to determine the factors responsible for lapses in safety or data quality.<\/p>\n

Features of SAS JMP Statistical Discovery Software:<\/span><\/h3>\n