Online Training - Clinical SAS (Base SAS, Advance SAS and Biostatistics) with Project Experience Certification & Placement Assistance
BioMed Informatics Medwin Hospitals, Hyderabad, India is a leading Clinical Research Organization offering best SAS Training in Hyderabad since the year of 2000. Online SAS Training in Hyderabad, India includes best Clinical SAS Training online (Base SAS Programming course certification, Advance SAS Programming course certification and Biostatistics) to find out efficacy and safety of Investigational Product. BioMed Informatics Medwin Hospitals Online Training complimented as the best Clinical SAS Training in USA, best Clinical SAS Training in UK, best Clinical SAS Training in Australia, best Clinical SAS Training in Germany, best Clinical SAS Training in Sweden, best Clinical SAS Training in Netherlands, best Clinical SAS Training in Singapore, best Clinical SAS Training in Europe, best Clinical SAS Training in Canada. SAS (Statistical Analysis Software) was primarily developed by SAS Institute for the data management analysis. SAS Clinical Training online helps you gain the analytical skills to apply in Clinical studies. SAS Clinical online training course provides insights on developing the SAS programming to conduct analysis for the different types of clinical trials and new drug applications. With best Practical Hands on Live online Clinical SAS Programming Training, Analysts play predominant role in evaluation of drugs in clinical studies. Globally most of the Companies representing IT, Healthcare, Pharmaceutical, Biotechnology, SMO and Contract Research Organizations (CRO) have relied on SAS Programming to interpret the data. It is very difficult to draw a concrete conclusion from Clinical Research because of inherent differences between two individuals and also from group to group. The extent of this variability in a character is by way of chance, i.e., biological or normal is revealed by statistical methods. Interpretation, drawing conclusions and recommendations play a major role in Clinical Research.
SAS Certification Training
SAS Certification Training is intended to make you an expert in Base SAS Certification Training, Clinical SAS Certification Training, Advanced SAS Certification Training, SAS Clinical Certification Training, Biostatistics SAS Certification Training and Data analytics. SAS primarily comprises of Reading Data, Analysing Data and Reporting.
SAS Programming is used to find out Safety and Efficacy of Investigational Product (IP) in Clinical Research. SAS Programmers are required through the entire life cycle of a drug - starting at the preclinical development stage and going right through to continued monitoring of drugs once they hit the market.
If you're looking to boost your career prospects in the pharmaceutical industry, SAS training is a great string to add to your bow. Whether you want to move into clinical research or enhance your profile in your existing company, SAS training is crucial. Compliance to European and American Data regulations is important.
Brexit and implementation of the new regulatory base of Clinical Data in the UK, as well as in the Eurasian Economic Union (EAEU) countries, have transformed Clinical Data to a key element brought to the attention of all pharmaceutical industry players. For years, a globally harmonized approach to Clinical Data has been discussed as a concept for integrated regulations. Considering the recent developments, we are Getting Closer Harmonized systems.
SAS Certification Training Online
Looking for professional SAS Certification training? If you hold an associate's degree or higher and want to advance your career in Clinical SAS, our Online Training - Clinical SAS (Base SAS, Advance SAS and Biostatistics) with Practical Hands on Training with Flexible Timings & Project Experience Certification with Placement Assistance is right for you to boost your career. Our SAS Certification training online focuses on ICH-GCP/FDA (US)/EMEA (Europe, the Middle East and Africa)/Canada (Health Canada)/TGA (Australia)/MHRA (UK) guidelines, and hands-on training. Unique program designed for professionals aspiring to make a career in Pharmaceutical industry using the in-demand, industry-based SAS Statistical Software.
Online Training Features
- Web based classroom
- One faculty/student
- Placement support
- Regular/Fast track/Weekend individual slot
- Flexible timings
- Training Mode: Skype/Teamviewer
Certification
Course Certificate & Job Experience Certificate would be awarded at the end of the program.
Course Curriculum
SAS Modules
- SAS / BASE
- SAS / STAT
- SAS / REPORT
- SAS / ODS
- SAS / GRAPH
- SAS / ACCESS
- SAS / CONNECT
- SAS / SQL
- SAS / MACROS
- LIVE SAS CLINICAL PROJECT
SAS BASE
- Introduction to SAS System & Architecture
- SAS Windowing Environment
- SAS Libraries
- Variables & SAS Syntax Rules
- Data Step and Proc Step
- Titles & Footnotes
- Proc Print Statement
- Proc Print Options
- Set Statement
- Dataset Options
- Options Statement
- Types of Input Statements
- Infile Statement With Options
- Keep, Drop and Rename Statements
- Update Statement
- Modify Statement
- Merging Concepts
- Interleaving Concept
- Logical Variables
- Retain Statement
- Formats and Informats
- Conditional Statements
- SAS Functions
- Do Statement
- Randomization
BASE SAS PROCEDURES
- Proc Sort
- Proc Append
- Proc Transpose
- Proc Contents
- Proc Format
- Proc Import
- Proc Export
- Proc Compare
- Proc Copy
- Proc Options
- Proc Forms
- Proc Datasets
- Proc Printto
- Proc Calendar
BIOSTATISTICS
- Introduction To Biostatistics - Clinical Applications
- Frequency Distribution Of Clinical data
- Clinical Data Presentation
- Measures Of Centering Constants
- Measures Of Dispersion
- Normal Distribution
- Null Hypothesis / Alternate Hypothesis
- p - Value Interpretation
- Sampling Variation
- Probability Concepts In Clinical Trials
- t-Test - Pharma Applications
- Chi Square test - Adverse Event Analysis
- Correlation & Regression - Estimation Analysis
- ANOVA - Efficacy Analysis
SAS / STAT (DATA ANALYSIS)
- Proc Means (mean, median, std, n, var, cv, range, q, q3, qrange, p50)
- Proc Univariate
- Proc Summary
- Proc TTest (Paired and Unpaired)
- Proc Anova (One Way, Two Way and Manova)
- Proc Glm
- Proc Freq
- Proc Chisq
- Proc Corr
- Proc Reg
SAS / GRAPH
- Proc Plot
- Proc Gplot
- Mutliple Plots & Overlay
- Symbol Statement
- Title and Footnote Statements
- Proc Chart
- Proc Gchart
- Vertical, Horizontal, Pie
- Group, Subgroups
- Proc G3D
- Proc Gprint
- Graph-N-Go
SAS / REPORT
- Proc Report
- Column Statements
- Break/Rbreak Statements
- Compute Statement
- Frequency Procedure
- Proc Tabulate
- One-Dimensional Tables
- Two-Dimensional Tables
- Summary Statistics
SAS / ODS
- ODS Statements
- ODS Options
- Using ODS to Create HTML, PDF, RTF
- Proc Template
- Proc Report with ODS
SAS / SQL
- Introduction to SAS/SQL
- Proc Sql Statements
- Proc Sql Options
- Set Clause
- Where Clause
- Order by Clause
- Group by Clause
- Having Clause
- Distinct Clause
- Formatting Output
- Case Expression and Conditional Logic
- Sql Set Operators
- Joins in Sql
- Creating ,Populating & Deleting Tables
- Alter Table Statement
- Renaming A Table & Columns
- Changing Column's Length
- Aggregate Functions
- Pass Through Facility
SAS / MACROS
- Macro Concepts
- Macros And Macro Variables
- Creating Macro Variables
- Using Macro Variables
- Invoking A Macro
- Passing Arguments to Macros
- Macro Quoting Functions
- Macro Options
- Macro Expressions
SAS / ACCESS
- Import & Export Procedures
- Proc Access
- Worksheet Statement
SAS / CONNECT
- Cimport Procedure
- Cport Procedure
- Using Select Statement
LIVE SAS CLINICAL PROJECT
You will be extensively involved in
- Extracting the data from various internal and external databases (Oracle, MS Access, Excel spreadsheets) using SAS/ACCESS, SAS/INPUT
- Developing programs for converting the Oracle data into SAS datasets using SQL Pass Through Facility
- Clinical trial data analysis with different Statistical Procedures
- Using various statistical procedures to find out the efficiency of the drug as per 21 CFR USFDA Guidelines
- Interpretation of p-value and drawing conclusions
- Assigning subjects to different treatment arms with SAS Randomization Programs
- Creating the reports using the SAS procedures and using ODS statements to generate different output formats like
- HTML, PDF, RTF and excel to view them in the web browser
- Creating the statistical reports using Proc Report, Proc Tabulate and SAS Macro
- Thorough understanding of Protocol, Statistical Analysis Plan (SAP)
- Analyzing the data and creating tables according to the Statistical Analysis Plan (SAP)
- Generating the demographic tables, adverse events and serious adverse events reports
- Using the SAS procedures (MEANS, FREQ, SUMMARY, TRANSPOSE, TABULATE, REPORT etc) and SAS/STAT procedures (REG, CORR, GLM, ANOVA and UNIVARIATE etc.) for summarization, cross-tabulations and statistical analysis
- Manipulation of SAS datasets using SET, MERGE, UPDATE, MODIFY and Conditional statements
- Generating Graphs and Figures using PROC CHART, PROC GCHART, PROC PLOT, PROC GPLOT and Graph-N-Go
- Validation and QC of the efficacy and safety tables
- Using PROC EXPORT and Export wizard to Transfer SAS data to external data sources
- Providing programming support for the creation and maintenance of programs used in Data Management, Data Validation, Data Cleaning and Statistical Report Generation
- Extensive Applications in SAS/SQL, SAS/ACCESS, SAS/CONNECT and SAS Macros
- Generating Tables, Listings, Figures/Graphs (TLFs or TLGs)
- Working with datasets such as DM (Demographics), LB (Laboratory), MH (Medical History), AE (Adverse Events), VS (Vital Signs), CM (Concomitant Medication)
- Manipulation and Reporting of clinical data using PROC SQL
- Extensive programming in writing and debugging the Macro routines and applying Macro variables in SAS program
- CDISC Standards (SDTM, ADaM, LAB, ODM)
- Live SAS Clinical Projects
Global SAS Data Regulations
- Australia - Therapeutic Goods Administration (TGA)
- New Zealand - MEDSAFE
- North America
- Canada - Health Canada
- USA - FDA: Food and Drug Administration
- Central/South America
- Argentina - ANMAT
- Brazil - Agencia Nacional de Vigilancia Sanitaria (ANVISA)
- Chile - Instituto de Salud Publico (ISP)
- Columbia - Instituto Nacional de Vigilancia Medicamentos y Alimentos (INVIMA)
- Costa Rica - Ministerio de Salud
- Cuba - CECMED
- Dominican Republic - Direccion General de Drogas y Farmacias
- Jamaica - Ministry of Health
- Mexico - Comision Federal para la Proteccion contra Riesgos Sanitarios (COFEPRIS)
- Paraguay - Ministro de Salud Publica y Bienestar Social
- Peru - Ministerio de Salud
- Uruguay - Ministerio de Salud Publica
- European Union - EMA: European Medicines Agency
- Armenia - Scientific Centre of Drug and Medical Technology Expertise
- Austria - Agency for Health and Food Safety (AGES)
- Belgium - Federal Agency for Medicines and Health Products
- Bulgaria - Bulgarian Drug Agency
- Croatia - Agency for Medicinal Products and Medical Devices of Croatia
- Cyprus - Ministry of Health
- Czech Republic - State Institute for Drug Control
- Denmark - Danish Medicines Agency
- Estonia - State Agency of Medicines
- Finland - Finish Medicines Agency
- France - Agence Nationale de Securite du Medicament et des Produits de Sante
- Germany - Federal Institute for Drugs and Medical Devices
- Georgia - Regulation Agency for Medical and Pharmaceutical Activities
- Greece - National Organisation for Medicines
- Hungary - National Institute of Pharmacy
- Iceland - Icelandic Medicines Agency
- Ireland - Irish Medicines Board
- Italy - National Institute of Health
- Lithuania - State Medicines Control Agency
- Luxembourg - Ministry of Health
- Malta - Maltese Medicines Authority
- Moldova - Medicines Agency
- Netherlands - Medicines Evaluation Board
- Norway - Norwegian Medicines Agency
- Poland - The Office for Registration of Medicinal Products, Medical Devices and Biocidal Products
- Portugal - National Authority of Medicines and Health Products
- Romania - National Medicines Agency
- Russia - Ministry of Health of the Russian Federation
- Serbia - Medicines and Medical Devices Agency of Serbia
- Slovakia - State Institute for Drug Control
- Slovenia - Ministry of Health
- Spain - Spanish Medicines Agency
- Sweden - Medical Products Agency
- Switzerland - Swiss Agency for Therapeutic Products
- Ukraine - Ministry of Health
- United Kingdom - Medicines and Healthcare Regulatory Agency (MHRA)
- Bahrain - I-SEHA
- Egypt - Ministry of Health
- Iran - Ministry of Health
- Israel - Ministry of Health
- Jordan - Jordan Food and Drug Administration
- Lebanon - Ministry of Public Health
- Saudi Arabia - Saudi Food and Drug Authority
- United Arab Emirates - Ministry of Health
- Bangladesh - Directorate General of Drug Administration (DGDA)
- Bhutan - Drug Regulatory Authority
- China - CFDA/NMPA: State Food and Drug Administration
- India - Central Drug Standards Control Organization (CDSCO)
- Indonesia - POM (Pengawas Obat dan Makanan)
- JAPAN - PMDA: Ministry of Health, Labour and Welfare
- Korea (South) - Korean Food and Drug Administration (KFDA)
- Laos - Food and Drug Department
- Malaysia - Ministry of Health (MOH)
- Nepal - Department of Drug Administration
- Philippines - Department of Health (DOH)
- Singapore - Health Sciences Authority (HSA)
- Sri Lanka - Ministry of Health (MOH)
- Taiwan (Republic of China) - Taiwan Food and Drug Administration (TFDA)
- Thailand - Food and Drug Administration of Thailand
- Vietnam - Drug Administration of Vietnam
- Algeria - Ministry of Health and Population
- Botswana - Ministry of Health (MOH)
- Burkina Faso - Le Ministere de la Sante
- Ghana - Food and Drugs Authority
- Kenya - Pharmacy and Poisons Board
- Morocco - Ministry of Health
- Nigeria - National Agency for Food and Drug Administration and Control
- Rwanda - Ministry of Health
- Senegal - Ministere de la Sante et de l'Action Sociale
- South Africa - Medicines Control Council (MCC)
- Swaziland - Ministry of Health
- Tanzania - Tanzania Food and Drug Authority (TFDA)
- Uganda - National Drug Authority