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SAS CDM

SAS CDM Online Training

SAS Clinical Data Integration  organizes, standardizes and manages clinical research data and metadata.  It provides the foundation you need to ensure standard, trusted clinical data to support strategic analyses, such as cross-study and advanced safety analysis. With SAS, you can gain both speed and efficiency by automating repeatable clinical data integration tasks.

Clinical Trails and Clinical Data Management : 

  • Phase trails: preclinical1,2,3 and 4
  • Drug discovery and development
  • ICH GCP
  • Computer system validation
  • 21 CFR 11
  • CRF designing
  • Pharmacokinetics
  • Pharmacovigilance
  • Clinical data management process
  • CDISC introduction
  • CTM systems
  • Data management plan

Sub Chapter

  • General abbreviated terms
  • Introduction to clinical trails
  • Responsibilities of CRA
  • Activities of CRA in house
  • CRA monitoring
  • Clinical trail monitoring
  • Responsibilities of PI
  • IRB
  • Informed consent form
  • ICH history
  • GPC guidelines
  • FDA history
  • FDA guidelines
  • IND,NDA reviews
  • Clinical research study document
  • CRF reviews and sample CRF’s
  • CRF data submission
  • CRF receiving
  • Introduction to SAS in CDM

Components of SAS Different data types

  • Base/SAS
  • SAS/STAT
  • SAS/Graph
  • SAS/ACCESS
  • SAS procedures
  • SAS Procedures
  • SAS Macros
  • SAS (working with sql)

Open clinical

  • Data base design
  • Protocol planning
  • CRF Data entry
  • Data management
  • Study planning
  • Study design
  • Oracle clinical (overview)