SAS Clinical Course
Gain expertise in SAS for hypertension clinical trials. Master CDISC standards like SDTM and ADaM, construct ADSL and ADVS datasets, execute efficacy and safety analyses, identify TEAEs, and generate regulatory-compliant tables and listings for practical clinical research applications. This focused course equips you with essential skills for real-world pharmacovigilance and trial reporting in the pharmaceutical industry.

flexible workload of 4 to 360h
valid certificate in your country
What will I learn?
This SAS Clinical Course provides hands-on training to create SDTM and ADaM datasets, prepare ADSL, ADVS, ADAE, and ADLB files, and conduct hypertension efficacy and safety analyses. You will learn to programme change-from-baseline for blood pressure, generate TEAE flags, execute MMRM models, perform thorough quality checks, and produce regulatory-compliant tables, listings, and documents in a concise programme.
Elevify advantages
Develop skills
- Build SAS datasets for hypertension trials ready for regulatory submission as SDTM and ADaM.
- Perform clinical trial analyses by coding ITT, PP, and safety populations with primary endpoints in SAS.
- Model blood pressure efficacy using MMRM, baseline changes, and Week 12 outputs efficiently in SAS.
- Analyse safety data by deriving TEAEs, SOC/PT summaries, and detailed AE listings in SAS.
- Develop QC and audit capabilities with SAS validation checks, logs, and metadata for compliant submissions.
Suggested summary
Before starting, you can change the chapters and the workload. Choose which chapter to start with. Add or remove chapters. Increase or decrease the course workload.What our students say
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