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eSub | What you should know for eCRT package submitted to FDA (Statistical Programming \u0026 Life) View |
FDA guide for submitting SAS programs | optimize your programming set-up from the beginning (Statistical Programming \u0026 Life) View |
What is an FDA pre-submission (Medical Device Academy) View |
FDA's Bioresearch Monitoring (BIMO) Program: Inspection of Sponsors, CROs, and Monitors (Kathy Barnett) View |
Clinical Data Interchange Standards (CDISC), Part 1 of 4 (NIH VideoCast) View |
FDA's Bioresearch Monitoring (BIMO) Program Trailer (Kathy Barnett) View |
cSDRG: Basic introduction to SDTM Clinical Study Data Reviewers guide (mycsg) View |
Clinical Data Interchange Standards (CDISC), Part 2 of 4 (NIH VideoCast) View |
SASS Data Population - (Module E) - Submission Validations (CSIS Training Channel) View |
How to become a statistical programmer in CRO vs Pharmaceutical Industries (Statistical Programming \u0026 Life) View |