SAS CDM Online Training

 >>  SAS CDM Online Training

SAS CDM Online Training


 (4.9) | 750 Ratings


Introduction


SAS CDM Online Training Details
Track Regular Track Weekend Track Fast Track
Course Duration 30 Hrs 8 Weekends 5 Days
Hours 1hr/day 2 Hours a day 6 Hours a day
Training Mode Online Classroom Online Classroom Online Classroom
Delivery Instructor Led-Live Instructor Led-Live Instructor Led-Live


Course Curriculum

SAS CDM Online Training Details

Module 1: SAS Programming

Topics: Base SAS, Create SAS Variables and Subset Data, Read Different Types of Data into SAS Data Sets Navigate the SAS Windowing Environment, Combine SAS Data Sets, Validate and Clean SAS Data Sets, Make and Raise Listing and Summary Reports.

Module 2: Data Manipulation Techniques

Topics: Transform Date Variables, Numeric, and Date Variables, Perform SAS Array Processing and Do Loop, Control SAS Data Set Input and Output, Read and Summarize Different Types of Data

Module 3: SAS Macro Language

Topics: Automate and Customize The Production of SAS Code, Macro Variables and Macro Functions, Text Substitution in SAS Code, Construct SAS Code

Module 4: SAS SQL

Topics: Summarize and Present Data, Query and Subset Data, Combine Tables, Create and Modify Table Views and Indexes, Replace Multiple Data and Proc Steps with One SQL Query, Including Complex Joins and Merges

Module 5:SAS Graph

Topics: Design Graphs, Customize Default Graph Elements, Apply Annotations, Deliver Graphs in Multiple Formats

Module 6: SAS Report Writing

Topics: Create Summary Reports Based on Across, Class Variables or Group Using Proc, Create Tabular Detail Report Using Proc Report, Detail Reports with Computed Column, Grand Totals and Subtotals

Module 6: Processing Spreadsheet Data And Database With SAS

Topics: Generate Efficiency Techniques for Optimizing Data Access Performance, Connect Data Using the SQL Procedure and the Data Step, Export Data Using the Export Wizard, Import Excel Data and Microsoft Access Using the Import Wizard, Utilizing the SQL Pass-Through Facility and LIBNAME Statement for Reading Data in Excel Workbooks and Relational Databases

Module 7: SAS Clinical Data Integration

Topics: Register Source Data and Target Tables, Customize Clinical Domain Tables and Columns, Promote New Standards, Monitor Clinical Projects, Import Clinical Standards Into Metadata, Generate Jobs and Search the Functionality of the Job Editor, Generate Define.Xml Files for Cdisc Clinical Submissions, Make, Load and Verify Contents and Structures of Clinical Domain Target Tables

Module 8: Open Clinical

Topics: Overview of Oracle Clinical, Database Design, Data Management, CRF Data Entry, Study Design, Study Planning, Protocol Planning

Module 9: Clinical Trails And Clinical Data Management

Topics: Clinical Data Management Process, Data Management Plan, CTM Systems, 21 Cfr 11, Cdisc Introduction, Pharmacovigilance, Drug Discovery and Development, Computer System Validation, Pharmacokinetics, Phase Trails: Preclinical1,2,3 And 4, CRF Designs, Ich GCP

Module 10: Miscellaneous Sub Topics

Topics: Responsibilities of CRA, Clinical Trial Monitoring, CRA Monitoring, Activities of CRA In House, General Abbreviated Terms, Informed Consent Form, NDA and IND, Reviews, Clinical Research Study Document, Introduction To SAS In Cdm, Responsibilities Of PI, ICH History, IRB, FDA History and Guidelines, GPC Guidelines, CRF Reviews And Sample CRF’S, CRF Data Submission and Receiving

SAS CDM project

Exam & Certification

0

Course Review

(4.9)
5 stars
4 stars
3 stars
2 stars
1 stars

Course Curriculum

SAS CDM Online Training Details

Module 1: SAS Programming

Topics: Base SAS, Create SAS Variables and Subset Data, Read Different Types of Data into SAS Data Sets Navigate the SAS Windowing Environment, Combine SAS Data Sets, Validate and Clean SAS Data Sets, Make and Raise Listing and Summary Reports.

Module 2: Data Manipulation Techniques

Topics: Transform Date Variables, Numeric, and Date Variables, Perform SAS Array Processing and Do Loop, Control SAS Data Set Input and Output, Read and Summarize Different Types of Data

Module 3: SAS Macro Language

Topics: Automate and Customize The Production of SAS Code, Macro Variables and Macro Functions, Text Substitution in SAS Code, Construct SAS Code

Module 4: SAS SQL

Topics: Summarize and Present Data, Query and Subset Data, Combine Tables, Create and Modify Table Views and Indexes, Replace Multiple Data and Proc Steps with One SQL Query, Including Complex Joins and Merges

Module 5:SAS Graph

Topics: Design Graphs, Customize Default Graph Elements, Apply Annotations, Deliver Graphs in Multiple Formats

Module 6: SAS Report Writing

Topics: Create Summary Reports Based on Across, Class Variables or Group Using Proc, Create Tabular Detail Report Using Proc Report, Detail Reports with Computed Column, Grand Totals and Subtotals

Module 6: Processing Spreadsheet Data And Database With SAS

Topics: Generate Efficiency Techniques for Optimizing Data Access Performance, Connect Data Using the SQL Procedure and the Data Step, Export Data Using the Export Wizard, Import Excel Data and Microsoft Access Using the Import Wizard, Utilizing the SQL Pass-Through Facility and LIBNAME Statement for Reading Data in Excel Workbooks and Relational Databases

Module 7: SAS Clinical Data Integration

Topics: Register Source Data and Target Tables, Customize Clinical Domain Tables and Columns, Promote New Standards, Monitor Clinical Projects, Import Clinical Standards Into Metadata, Generate Jobs and Search the Functionality of the Job Editor, Generate Define.Xml Files for Cdisc Clinical Submissions, Make, Load and Verify Contents and Structures of Clinical Domain Target Tables

Module 8: Open Clinical

Topics: Overview of Oracle Clinical, Database Design, Data Management, CRF Data Entry, Study Design, Study Planning, Protocol Planning

Module 9: Clinical Trails And Clinical Data Management

Topics: Clinical Data Management Process, Data Management Plan, CTM Systems, 21 Cfr 11, Cdisc Introduction, Pharmacovigilance, Drug Discovery and Development, Computer System Validation, Pharmacokinetics, Phase Trails: Preclinical1,2,3 And 4, CRF Designs, Ich GCP

Module 10: Miscellaneous Sub Topics

Topics: Responsibilities of CRA, Clinical Trial Monitoring, CRA Monitoring, Activities of CRA In House, General Abbreviated Terms, Informed Consent Form, NDA and IND, Reviews, Clinical Research Study Document, Introduction To SAS In Cdm, Responsibilities Of PI, ICH History, IRB, FDA History and Guidelines, GPC Guidelines, CRF Reviews And Sample CRF’S, CRF Data Submission and Receiving

SAS CDM project

    Click here for Help and Support: info@sacrostectservices.com     For Inquiry Call Us:   +91 996-629-7972(IND)

  +91 996-629-7972(IND)
X

Quick Enquiry

X

Business Enquiry