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Basic
Getting Beyond Spreadsheet Analytics with Visual Data Discovery
31 March | 11:00 BST (12:00 CEST)After your data is prepared for analysis, use JMP to interactively explore, uncover hidden relationships, and start understanding your data. Learn how to uncover relationships visually to identify and correct missing information, review key summary statistics, and examine subsets of interest uncovered during exploration. See a 30-minute demo and stay on if you want to join 15-30 minutes of Topic Discussion and Q&A.
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Basic
JMP Clinical 17 Overview: A Refreshed Approach to Automated and Interactive Clinical Trial Reviews
20 April | 16:00 BST (17:00 CEST)JMP Clinical 17 provides fast, interactive, and easy to use tools for clinical trial safety review, medical monitoring, medical writing, and study monitoring. This new JMP-based version offers offer a fast and simple interface. See an overview of JMP Clinical’s capabilities for exploring and identifying important safety issues and documenting those issues for communicating with regulatory agencies.
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Basic
Easy DOE: Guiding New Users Through Designing and Analyzing an Experiment
21 April | 11:00 BST (12:00 CEST)See how to use design and analyze and experiment using a sequence of tabs, reports and profilers to flow you through the steps. Learn how to use the simple Guided Mode interface, understand the defaults for each step and how they depend on choices made in previous steps, interpret hints that guide decisions at each step, and how to move back and forth between steps. See how save work in a new .jmpdoe format that retains data and meta-data.
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Basic
Using JMP Clinical 17 for Medical Monitoring and Subject-Level Reviews in Clinical Trials
27 April | 16:00 BST (17:00 CEST)One of the most significant roles of the Medical Monitor is conducting safety data reviews to evaluate the presence or lack of safety issues with respect to the treatment the subjects receive. Reviews are conducted throughout the study, from Phase 1 through Phase 4. Not only are reviews required by regulators, but they are necessary to ensure the safety of participants. By following subjects as they progress through the study, researchers can build a picture of the safety profile of the compound under consideration. See an example of how Medical Monitors can use JMP Clinical to discover and understand the causes of adverse safety events in a clinical trial using several JMP Clinical 17 study-level and subject-level data views.
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Basic
Process Optimization with DoE and Design Space Profiler
26 May | 11:00 BST (12:00 CEST)See how to describe the goal, specify effects for an assumed model, generate a design, collect experimental run data, create, and fit a model incorporating experimental data, and use factors to optimize and improve settings. With Design Space Profiler, interactively find limit of failure regions (operational ranges) inside the factor space where the model(s) predict that the response(s) will be within specification.
Prerequisites to get the most from Mastering JMP:
