This course is specifically designed to meet the analytical needs of those individuals working within FDA regulated industries. Areas of focus include: JMP basics, analysis of data for basic engineering and scientific applications including statistics, distribution analysis, capability assessment, variation analysis, comparison tests, sample size selection, hypothesis testing, confidence intervals and multiple factor modeling. The course requires 24 hours of instruction.
This course is required for all scientists, engineers and quality professionals who actively work on all aspects of discovery, product and process development where the goal is to characterize, optimize and improve product and process performance.
There are no prerequisites for this course.
Table commands
Column commands
Row commands
Subset commands
Saving Scripts, Journals and Projects
Measures of center and spread
Standard error and central limit theorem
Normal distribution
t distribution and confidence intervals
Test for normality
Individuals and tolerance intervals (normal)
Process capability (normal)
Nonnormal distribution fitting and process capability
Contour plots, Components of Variance, REML and POV
Sample size for the mean and standard deviation
t test – one sample
t test – two sample
Test for differences in variances
t test – paired
One-way ANOVA and F test
N-way ANOVA
Nonparametric data analysis (optional)
Simple linear regression, correlation
Multiple regression
ANCOVA
Mean and sigma for proportion defective
Sample size and statistical tests for proportion defective
Mean and sigma for defect per unit
Chi-square test for defects and proportion defective
Pareto graphs and cross tabs analysis
Logistic regression
Nominal logistic regression (optional)
Recursive partitioning
Nonlinear modeling, growth and EC50 determination