CLINICAL TRAIL PROJECT Online Training

1.Understanding CRF(Case Report Form).
2.Protocol
3.SAP (Statistical Analysis Plan)
4.Mocks (Mock Shells)
5.Specs (Specifications)
6.Classifying clinical trial data 
7.Understanding Issue log
8.MOM (Minutes of Meeting)
9.SOP(Standard Operating Procedures)
10.SAS programming guidelines
11.Study populations
12.study day calculation
13.Windowing data
14.Transposing data 
15. LOCF 
16.Change from baseline
17.Creating Safety tables
18.Creating Efficacy tables 
19.Creating Shift tables
20.Creating listing report 
21.Validation and QC checks
22.Creating ADS

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