Clinical SAS Programming Training Demo Video | SAS Programming Online Course - GOT
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Description: Clinical SAS Programming Training is used for clinical data integration. Clinical SAS Programming Online Training enhances usability by adding new metadata.
Clinical SAS Programming Training Introduction:
Clinical SAS Programming Training is used for clinical data integration, standardizing, organizing and managing clinical research data and metadata.Global Online Trainings offers online Clinical SAS Programming Online Training for supporting all its participants in achieving promptness and competence by mechanizing repeatable clinical data integration projects.This is a new product offering from SAS that focuses on pharmaceutical industry needs for managing, verifying and transforming the creation of industry mandated data standards such as the Clinical Data Interchange Standards Consortium.This project is coordinated by best subject matter experts and Clinical SAS Programming tutorials
CLINICAL SAS PROGRAMMING ONLINE TRAINING COURSE CONTENT :
TOPIC 1: ENVIRONMENT & GUIDING PRINCIPLES
Clinical SAS Programming Training Overview
TOPIC 2: THE STATISTICAL PROGRAMMERS WORKING ENVIRONMENT
Statistical Programmer Work Description
Drug/Device Development Process
Industry Regulations & Standards
Your Clinical Trial Colleagues
Guide the Principles for Statistical Programmer
Understand the Clinical SAS Programming Training Study
Program a Task Once & Reuse Your Code Everywhere
Clinical Trial Data are Dirty
Use the SAS Macros Judiciously
A Good Programmer Is a Good Student
Strive to Make Your Program Readable
TOPIC 3: PREPARING & CLASSIFYING THE CLINICAL TRIAL DATA
TOPIC 4: PREPARING THE CLINICAL TRIAL DATA
“Clean” Data If They Are Needed for Analysis
Categorize Data If Necessary
Avoid the Hardcoding Data
TOPIC 5: CLASSIFYING THE CLINICAL TRIAL DATA
Demographics & Trial-Specific Baseline Data
Concomitant or Prior Medication Data
Medical History Data
Investigational the Therapy Drug Log
Laboratory Data
Adverse Event Data
Endpoint/Event Assessment Data
Clinical Endpoint Committee Data
Study Termination Data
Treatment Randomization Data
Quality of life Data
TOPIC 6: IMPORTING THE DATA
TOPIC 7: IMPORTING RELATIONAL DATABASES & CLINICAL DATA MANAGEMENT SYSTEMS
SAS/ACCESS SQL Pass through Facility
SAS/ACCESS LIBNAME Statement
TOPIC 8: IMPORTING THE ASCII TEXT
PROC IMPORT & the Import Wizard
SAS DATA Step
SAS Enterprise Guide
TOPIC 9: IMPORTING THE MICROSOFT OFFICE FILES
LIBNAME Statement
Import Wizard & PROC IMPORT
SAS/ACCESS SQL Pass-Through Facility
SAS Enterprise Guide
TOPIC 10: IMPORTING XML
XML LIBNAME Engine
SAS XML Mapper
PROC CDISC
TOPIC 11: IMPORTING FILES IN OTHER PROPRIETARY DATA FORMATS
TOPIC 12: TRANSFORMING DATA & CREATING ANALYSIS DATASETS
TOPIC 13: KEY CONCEPTS FOR CREATING ANALYSIS DATASETS
Defining the Variables Once
Defining Study Populations
Defining Baseline Observations
Last Observation Carried Forward
Defining the Study Day
Windowing Data
Transposing Data
Categorical Data and Why Zero & Missing Results Differ Greatly
Performing Many-to-Many Comparisons/Joins
Using Medical Dictionaries
Other Tricks & Traps in the Data Manipulation
TOPIC 14: COMMON ANALYSIS DATA SETS
Critical Variables Data Set
Change from baseline Data Set
Time to Event Data Set
TOPIC 15: CREATING TABLES & LISTINGS
TOPIC 16: CREATING TABLES
General Approach to Creating Tables
A Typical Clinical Trial Table
Using the PROC TABULATE to Create Clinical Trial Tables
Using the PROC REPORT to Create Clinical Trial Tables
Creating the Continuous/Categorical Summary Tables
Creating the Adverse Event Summaries
Creating the Concomitant or Prior Medication Tables
Creating a Laboratory Shift Table
Creating the Kaplan Meier Survival Estimates Tables
TOPIC 17: CREATING LISTINGS: OUTPUT APPEARANCE OPTIONS AND ISSUES
Creating ASCII Text Output
Creating Rich Text Format (RTF) Output
Creating Portable Document Format (PDF) Files
“Page X of N” Pagination Solutions
Footnote Indicating SAS Program & Date
TOPIC 18: SAS MACRO BASED REPORTING SYSTEMS
Clinical SAS Programming Training Reporting Systems
TOPIC 19: CREATING THE CLINICAL TRIAL GRAPHS
TOPIC 20: COMMON CLINICAL TRIAL GRAPHS
Scatter Plot
Line Plot
Bar Chart
Box Plot
Odds Ratio Plot
Kaplan Meier Survival Estimates Plot
TOPIC 21: SAS TOOLS FOR CREATING THE CLINICAL TRIAL GRAPHS
Common Clinical Trial SAS/GRAPH Procedures
Using the Annotate Facility for Graph Augmentation
TOPIC 22: SAMPLE GRAPHS
Creating a Scatter Plot
Creating a Line Plot
Creating a Bar Chart
Creating a Box Plot
Creating an Odds Ratio Plot
Creating a Kaplan Meier Survival Estimates Plot
TOPIC 23: OUTPUT OPTIONS
Selecting Graphics Drivers
Using the ODS Destinations for the SAS/GRAPH