JMP Clinical 3.0 adds the ability to drill down to patient level data from study level data with the new patient profile feature. Additionally, the JMP starter menu allows for customization and standardization of analysis via the workflow builder. Learn more about these features and more.
Overview
JMP Clinical software from SAS shortens the drug development process by streamlining safety reviews during clinical trials. Dynamically linking advanced statistics and graphics, JMP Clinical creates reports from CDISC data, the global standard, helping reviewers migrate into the modern review environment. It combines JMP, already the tool of choice for medical reviewers, and SAS, the standard analysis and reporting tool for biostatisticians in the pharma industry.
SAS Publishing Representatives are available in the U.S. from 8-5 ET to answer your documentation questions. Contact us at 1-800-727-3228 or e-mail.
For additional information, please visit the JMP Training Homepage
Need help?
Curriculum consultants are available in the U.S. from 9-5 EST. Contact us at 1-800-333-7660 or e-mail.
International customers, please contact your country office.
Need help?
Visit the JMP Support Page to access various self-help and assisted-help resources or submit a problem through the SAS Technical Support Form.