Showing posts with label SAS Clinical online training. Show all posts
Showing posts with label SAS Clinical online training. Show all posts

Monday, 16 May 2016

SAS Clinical Online training

 In this online course, you will learn nuts and bolts and propelled SAS clinical programming ideas to peruse and control clinical information. Utilizing the clinical elements and essential SAS Clinical programming ideas of clinical trials, this course demonstrates to import ADAM, CDISC or different principles for space structure and substance into the metadata, fabricate clinical area target table metadata from those norms, make occupations to stack clinical areas, to approve the structure and substance of the clinical spaces in light of the models, and to produce CDISC standard define. xml records depicting the space tables for clinical entries.




Clinical Features 

Individuals with herpes zoster most regularly have a rash in maybe a couple contiguous dermatomes (restricted zoster). The rash most usually shows up on the storage compartment along a thoracic dermatome. The rash does not normally cross the body's mid-line. In any case, around 20% of individuals have rash that covers contiguous dermatomes. Less generally, the rash can be more boundless and influence three or more ddermatomes.. This condition is called dispersed zoster. This by and large happens just in individuals with bargained or smothered invulnerable frameworks. Scattered zoster can be hard to recognize from varicella.

The rash is typically excruciating, irritated or tingly. These manifestations may go before rash onset by days to weeks. Some individuals may likewise have cerebral pain, photophobia (affectability to brilliant light), and discomfort in the prodromal stage.

The rash forms into groups of clear vesicles. New vesicles keep on forming more than three to five days and dynamically dry and outside layer over. They for the most part mend in two to four weeks. There might be perpetual pigmentation changes and scarring on the skin.

BASE SAS and Advance SAS:

Basic SAS Concepts
Referencing files, setting Options, Editing and debugging SAS Programs
Creating List Reports and Enhanced List and summary reports
Creating SAS data sets from raw data
Understanding DATA step processing
Creating and applying user defined formats
Producing descriptive Statistics
Creating and managing variables
Reading SAS Data sets
Combining SAS data sets
Transferring Data with SAS functions
Generating Data with DO loops and processing variables with Array
Reading Raw Data in fixed fields
Advanced Base/SAS: Macros and Proc Sql
Advanced Base/SAS: Certification Steps

Friday, 22 April 2016

SAS Clinical Online Training

In this online course, you will learn fundamentals and propelled SAS clinical Online training programming ideas to peruse and control clinical information. Utilizing the clinical elements and fundamental SAS programming ideas of clinical trials, this course demonstrates to import ADAM, CDISC or different guidelines for space structure and substance into the metadata, construct clinical area target table metadata from those norms, make occupations to stack clinical areas, to approve the structure and substance of the clinical areas in view of the models, and to create CDISC standard define. xml records portraying the area tables for clinical entries.



Advantages 

Increment operational proficiency while bringing down expenses

Automate repeatable errands to free up assets for more esteem included undertakings.

Increase your ability to handle extra (and more mind boggling) worldwide trials.

Write and approve less code, and conceivably reuse code in future trials.

Scale clinical studies without including costly, elusive headcount.

Support versatile trials through quick access to clinical information for between time examination.

Reuse the work of others through a typical storehouse that empowers the administration and reuse of data, in this manner lessening both advancement and support time.


Clinical Trials Process
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 Form.
Describe regulatory requirements (principles of 21 CFR Part 11, International Conferenceon
Harmonization, Good Clinical Practices).
Clinical Trials Data Structures
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.
Import and Export Clinical Trials Data
Apply regulatory requirements to exported SAS data sets (SAS V5 requirements).
Manage Clinical Trials Data
Access DICTIONARY Tables using the SQL procedure.
Examine and explore clinical trials input data (find outliers, missing vs. zero values, etc).

Transform Clinical Trials Data
Apply categorization and windowing techniques to clinical trials data. Transpose SAS data sets.