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Statistical analysis of the generated clinical study data is essential for regulatory submission. The SAS generated data is required as mandatory for FDA WHO and some other ROW regulatories. I can provide the SAS generated reports of the clinical study data provided by using various statistical tools (such as ANOVA, students t test, Chi square test etc.). I can provide you a complete report in accordance with GCP and ICH E3 procedures.
Programming language:
Other
Technology:
Excel
•
SAS
Expertise:
Experiment design
•
Statistics
•
Regression testing
Tools:
Other