Itabhyas providing the best online training in clinical SAS technologies with the real time experts and certified professionals. Itabhyas training providing the best training to the student at their preferable timings and we will offer job support.
Faculty : Real Time Expert | Duration : 15hrs | Material : Yes | Price : Rs.12,000/-
Itabhyas online training is the Best Clinical SAS Online Training in USA, UK, Australia, Canada and India.
We offer Clinical SAS online training, which has a great trend in current software industry and helps the learners to enhance their comprehension with fresh information. We also offer them good quality tips to improve their acquaintance more in the software training courses and computer IT Training at online to contend with today competitive software world .
Statistical Analysis System is a type of integrated system provided by the SAS institute for the software products. Clinical SAS online training helps the programmers understand this software in detail and make use of this high performing software in completing the daily tasks of the office work. The SAS programs form the main basis of the Clinical SAS and define operation sequences that are to be performed on the data that are stored as tables. Even though there is non-programmer, graphical user interfaces such as SAS Enterprise Guide, these are usually only a front-end that facilitates or automates the Clinical SAS generation programs. Clinical SAS online training teaches the students or learners about how to access the Clinical SAS component functionalities via application programming interfaces that are prepared in the form of procedures and statements.
Who should do this course?
Professionals in data management, data warehousing or in a business intelligence role would find the certification ideal. In addition, recent college graduates having an inclination to logically solve problems and pursuing to enter the data analysis field will find the certification beneficial to kick start their careers. This course is also ideal, if you are a working professional OR a recent graduate who is.
- Aspiring to be in fast growing career
- Looking for a more challenging position
- Aiming to get into a more skillful role
- Aspiring to be one of the coolest scientists of 21st century
Clinical SAS Online Training batches will start every week. Make a call on +91-9030403937 or send a mail to firstname.lastname@example.org
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.
- Apply ‘observation carry forward’ techniques to clinical trials data (LOCF, BOCF, WOCF).
- Calculate ‘change from baseline’ results.
- Obtain counts of events in clinical trials.
Apply Statistical Procedures for Clinical Trials
- Use SAS procedures to obtain descriptive statistics for clinical trials data (FREQ, UNIVARIATE, MEANS, SUMMARY).
- Use PROC FREQ to obtain p-values for categorical data (2×2 and NxP test for association).
- Use PROC TTEST to obtain p-values for continuous data (one-sample, paired and two-sample t-tests).
- Create output data sets from statistical procedures.
Macro Programming for Clinical Trials
- 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).
Report Clinical Trials Results
- Use PROC REPORT to produce tables and listings for clinical trials reports.
- Use ODS and global statements to produce and augment clinical trials reports.
Validate Clinical Trial Data Reporting
- Explain the principles of programming validation in the clinical trial industry.
- Utilize the log file to validate clinical trial data reporting.
- Use programming techniques to validate clinical trial data reporting (PROC COMPARE, MSGLEVEL).
- Identify and Resolve data, syntax and logic errors.
- who is a trainer ?
IT Abhyas trainers are working professionals from the Industry and have 10 yrs of relevant experience.
- Will i ask for Demo session?
yes , we r conducting the demo sessions when u need.
- How i will practice ?
We will provide a software to do the practice.In case you come across any doubt, we have a 24*7 support team they will assist you.
- If I miss the session ?
Any situation you are not attend the session we will provide the Recorded session.
- What about the course Material?
We are ready to provide the course material.
- will i get the videos of course?
yes , you get the videos after completion of daily session.that access for life time.
- Will i enroll now take a sessions after?
yes you will join u take a sessions later.
- If i have any queries ?
you will send a mail or give a call to support team.