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|Components of the pharma industry||00:05:00|
|Phases of Clinical Trials||00:06:00|
|Data and reports in Clinical Trials||00:04:00|
|Types of data||00:05:00|
|Get to know the Clinical Study Documents|
|Get to know Clinical Study Documents – Section Overview||00:01:00|
|Study Documents – Clinical Study Protocol||00:03:00|
|The Inclusion- Exclusion Criteria||00:01:00|
|The Statistical Analysis Plan (SAP), mock shells, and Case Report Forms (CRFs)||00:04:00|
|Get to know Clinical Study Documents – Section Conclusion||00:01:00|
|Building the Clinical Study Reports (CSR)|
|Building the CSRs – Section Overview||00:02:00|
|General SAS Programming Steps||00:03:00|
|Understanding Demographics CRF||00:05:00|
|Understanding the Demographics Table||00:04:00|
|Planning to program the Demographics Table||00:06:00|
|Importing raw Demographics data into SAS||00:04:00|
|Deciding which PROCs to use||00:02:00|
|Deriving the AGE variable||00:11:00|
|Obtaining Summary Statistics for AGE||00:04:00|
|Adding the 3rd Treatment Group using Explicit Output||00:06:00|
|Deriving the SEX variable||00:04:00|
|Obtaining Summary Statistics for SEX||00:04:00|
|Concatenating the COUNT and PERCENTAGE variables||00:03:00|
|Deriving the RACEC variable||00:03:00|
|Obtaining Summary Statistics for RACE||00:03:00|
|Stacking all Statistics together||00:06:00|
|Fixing the precision points||00:04:00|
|Fixing the order of Statistical Parameters||00:06:00|
|Building the final report||00:02:00|
|Putting the final touches to the report||00:11:00|
|Building the CSRs- Section conclusion||00:01:00|
|Project Problem Statement||00:05:00|
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