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JMP® Clinical: Conducting Medical Safety Reviews of Clinical Trials

 

Understand the capabilities of JMP Clinical. Learn how to get started using JMP Clinical, build upon JMP templates, start creating your own templates, and determine if you have the right data.

 

See how to:

• Add study data
• View, add and update study data
• Profile subjects
• Create and share Adverse Event (AE and SAE) narratives and reports  
• Review safety-related results including distribution of demographics, Adverse Events and negative effects related to medication
• Customize report settings, create new report templates, and view and interpret reports
• Add and explore Oncology based reports
• Use JMP Clinical to list reports that are unavailable due to missing data
• Collect and prepare review data in a read-only format that can be shared with those who have JMP Clinical but who have no access to the particular study data

Resources:

• JMP Clinical CDISC Conversion Add-In with drag-and-drop interface to map JMP Data table columns to CDISC variables. It can be with or without JMP Clinical.
• JMP Clinical documentation, videos, blog posts, training options and customer stories.

Adverse EventsAdverse Events

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Tumor ResponsesTumor Responses

Other