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MindMajix

SAS Clinical Training

Introduction to SAS Clinical


SAS Clinical Data Integration 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 (CDISC). The product relies on SAS Data Integration
to provide centralized metadata management using the SAS
Metadata Server and the tools to visually transform data. SAS
Clinical Training enhances usability by adding new metadata
types, wizards and plug-ins that assist with clinically oriented
tasks.

Course Curriculum
Unit 1: Clinical Trials Process
Topics Describe the clinical research process (phases, key roles, key
organizations), Interpret a Statistical Analysis Plan, Derive programming
requirements from an SAP and an annotated Case Report, Describe regulatory
requirements (principles of 21 CFR Part 11, International Conference on
Harmonization, Good Clinical Practices)
Unit 2: Clinical Trials Data Structures
Topics - Identify the classes of clinical trials data (demographic, lab, baseline, concomitant

medication, etc.), Identify key CDISC principals and terms, Describe the structure and purpose
of the CDISC SDTM data model, Describe the structure and purpose of the CDISC ADaM data
model, Describe the contents and purpose of define.xml

Unit 3: Import And Export Clinical Trials Data


Topics Apply regulatory requirements to exported SAS data sets (SAS V5
requirements)
Unit 4:

Manage Clinical Trials Data

Topics - Access DICTIONARY Tables using the SQL procedure, Examine and explore clinical
trials input data (find outliers, missing vs. zero values, etc)

Unit 5: Transform Clinical Trials Data


Topics - Apply categorization and windowing techniques to clinical trials data

Transpose SAS data sets, Apply observation carry forward techniques to clinical trials data
(LOCF, BOCF, WOCF), Calculate change from baseline results, Obtain counts of events in
clinical trials
Unit 6: Macro Programming For Clinical Trials
Topics Create and use user-defined and automatic macro variables, Automate programs
by defining and calling macros, Use system options to debug macros and display values of
macro variables in the SAS log (MPRINT, SYMBOLGEN, MLOGIC, MACROGEN)
Unit 7: Report Clinical Trials Results
Topics - Use PROC REPORT to produce tables and listings for clinical trials
Reports Use ODS and global statements to produce and augment clinical trials reports

Our
SAS Clinical Online Training
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You can attend a DEMO for
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We Provide Online Training On


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We offers You
1.InteractiveLearningatLearnersconvenience
2. IndustrySavvy Trainers
3.Real Time"Practical scenarios
4. Learn Right from Your Place
5. Customized Course Curriculum
6. 24/7ServerAccess
7. Supportafter Training and Certification Guidance
8. Resume Preparation and Interview assistance
9. Recorded version of sessions

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Your feedback is highly important to improve our course
material.
For Free Demo Please Contact
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Email id: info@mindmajix.com
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