The Simplest Guide to Clinical Trials Data Analysis with SAS

سرفصل های دوره

1 - Introduction

1 - Clinical Trial Fundamentals.html

1 - Course Overview

2 - Components of the Pharma Life Science Industry

3 - Phases of Clinical Trials

4 - Data and Reports in Clinical Trials

5 - Types of data in Clinical Trials

6 - Section Conclusion

2 - Get to know the Clinical Study Documents

2 - Clinical Study Documents.html

7 - Get to know the Clinical Study Documents Section Overview

8 - Study Documents The Clinical Study Protocol

9 - The Informed Consent

10 - The Inclusion Exclusion Criteria

11 - The Statistical Analysis Plan SAP mock shells and Case Report Forms CRFs

12 - Get to know Clinical Study Documents Section Conclusion

3 - Building the Clinical Study Reports CSR

3 - Building the Demographics table.html

4 - Procedures and Variables.html

5 - Structuring Data.html

6 - Final Report.html

13 - Building the CSRs Section Overview

14 - SAS OnDemand Registration

15 - Loggingin to SAS after registration

16 - General SAS Programming Steps for building any CSRs

17 - Understanding the Demographics Case Report Form CRF

18 - Understanding the Demographics Table

19 - Planning to program the Demographics Table

20 - Importing raw Demographics data into SAS

20 - demog.xls

21 - Deciding which PROCs to use

22 - Deriving the AGE variable

23 - Obtaining Summary Statistics for AGE

24 - Adding the 3rd Treatment Group using Explicit Output

25 - Deriving the SEX variable

26 - Obtaining Summary Statistics for SEX

27 - Concatenating the COUNT and PERCENT variables

28 - Deriving the RACE variable

29 - Obtaining Summary Statistics for RACE

30 - Stacking all 3 Summary Statistics together

31 - Fixing the precision points

32 - Transposing data

33 - Fixing the order of statistical parameters

34 - Building the final report

35 - Putting the final touches to the report

35 - t-demog.zip

35 - t-demog-results.zip

36 - Building the CSRs Section Conclusion

4 - Final Project

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تولید کننده: Udemy-Training