Unit 01: Introduction |
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1.1 Components of the Pharma Industry |
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00:05:00 |
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1.2 Phases of Clinical Trials |
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00:06:00 |
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1.3 Data and Reports in Clinical Trials |
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00:04:00 |
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1.4 Types of Data |
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00:05:00 |
Unit 02: Knowledge on Clinical Study Documents |
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2.1 Clinical Study Protocol |
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00:02:00 |
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2.2 Ethical Consent |
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00:01:00 |
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2.3 Inclusion-Exclusion Criteria |
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00:01:00 |
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2.4 Statistical Analysis Plan: SAP, Mockshell and CRF |
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00:04:00 |
Unit 03: Developing the Clinical Study Reports |
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3.1 General SAS Programming Steps |
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00:02:00 |
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3.2 One Search Report: Demographics Table |
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00:04:00 |
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3.3 Understanding the Demographics Table |
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00:03:00 |
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3.4 Programming the Demographics Table |
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00:05:00 |
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3.5 Importing Raw Demographic Data into the SAS |
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00:04:00 |
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3.6 Deciding what Procedure to Use |
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00:02:00 |
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3.7 Deriving the AGE variable |
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00:10:00 |
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3.8 Obtaining Summary Statistics for AGE |
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00:04:00 |
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3.9 Adding the 3rd Treatment Group using Explicit Output |
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00:05:00 |
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3.10 Deriving the SEX variable |
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00:03:00 |
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3.11 Obtaining Summary Statistics for SEX |
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00:03:00 |
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3.12 Concatenating the COUNT and PERCENT Variables |
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00:03:00 |
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3.13 Deriving the RACE Variable |
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00:03:00 |
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3.14 Obtaining Summary Statistics for RACE |
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00:03:00 |
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3.15 Stacking All the 3 Summary Statistics Together |
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00:06:00 |
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3.16 Fixing the Precision Points |
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00:04:00 |
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3.17 Transposing Data |
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00:03:00 |
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3.18 Fixing the Order of Statistical Parameters |
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00:05:00 |
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3.19 Building the Final Report |
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00:02:00 |
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3.20 Putting the Final Touches to the Report |
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00:11:00 |
Resources |
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Resources – Clinical Data Management with SAS Programming |
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00:00:00 |
Assignment |
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Assignment -Clinical Data Management with SAS Programming |
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00:00:00 |