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Clinical SAS Project (CDISC/SDTM/ADaM/TLF)

The Clinical Data Interchange Standards Consortium (CDISC) is an open, multidisciplinary, neutral, non-profit standards developing organization (SDO) that has been working through productive, consensus-based collaborative teams, since its formation in 1997, to develop global standards and innovations to streamline medical research and ensure a link with healthcare. The CDISC mission is “to develop and support global, platform-independent data standards that enable information system interoperability to improve medical research and related areas of healthcare”.
Course: 6 Weeks

Certificate

Course Syllabus

Module 1: INTRODUCTION

  • INTRODUCTION ABOUT THE COURSE
  • INTRODUCTION ABOUT EACH DEPARTMENT (CLINICAL OPERATIONS, CDM, BIO-STATISTICS, MEDICAL WRITING)
  • DETAILED INFORMATION ABOUT BIO-STATISTICS (STATISTICIAN, STATISTICAL PROGRAMMERS, SAS PROGRAMMERS)
  • INTRODUCTION ABOUT CLIENT, REGULATORY BODIES, SUBMISSION OF THE STUDY
  • INTRODUCTION TO SPECIFICATIONS

Module 2: CDISC – SDTM

  • INTRODUCTION OF CDISC
  • WHY CDISC AND DATA STANDARDS
  • VERSIONS OF CDISC
  • IMPACT OF CDISC STANDARDS ON CLINICAL ACTIVITIES
  • CDISC MODELS
  • – STUDY DATA TABULATION MODEL (SDTM)
  • – ANALYSIS DATASET MODELS (ADaM)
  • – OPERATIONAL DATA MODEL (ODM)
  • FUNDAMENTALS OF SDTM
  • – WHAT IS SDTM?
  • – OBSERVATIONS AND VARIABLES IN SDTM
  • – SPECIAL PURPOSE DATASETS
  • – GENERAL OBSERVATION CLASSES IN SDTM
  • – SDTM STANDARD DOMAIN MODELS
  • – GENERAL ASSUMPTIONS FOR ALL DOMAINS
  • MODELS FOR SPECIAL PURPOSE DOMAINS
  • – DM, CO, SE, SV
  • DOMAIN MODELS BASED ON GENERAL OBSERVATION CLASSES
  • – INTERVENTIONS (CM, EX, EC, SU)
  • – EVENTS (AE, DS, MH, DV, CE)
  • – FINDINGS (LB, EG, VS, PE, IE, DD, DA)
  • – TRIAL DESIGN DOMAINS (TA, TE, TS, TI, TV)
  • SUPPLEMENTAL QUALIFIERS
  • SDTM MAPPING PROGRAMMING USING SAS
  • SDTM ANNOTATION ON CRF
  • SDTM MAPPING SPECIFICATIONS
  • REAL TIME PROJECT ON SDTM

Module 3: CDISC – ADaM

  • INTRODUCTION TO ADaM
  • WHY ADaM
  • KEY CONCEPTS
  • ADaM IMPLEMENTATION
  • FUNDAMENTALS OF THE ADaM STANDARDS
  • VARIABLES IN GENERAL
  • – ADSL VARIABLES
  • – BDS VARIABLES
  • – OCCDS VARIABLES
  • REAL TIME PROJECT ON ADaM
  • – ADSL, ADAE, ADCM, ADLB, ADVS ETC.

Module 4: TLFs (TABLES, LISTINGS, FIGURES)

  • INTRODUCTION TO CLINICAL TRIAL
  • SUMMARY REPORTS (TABLES, LISTINGS, FIGURES)
  • INTRODUCTION TO ICH E6, E9, E3
  • PROTOCOL
  • CRF / eCRF
  • SAP
  • MOCK SHELLS
  • INTRODUCTION TO STATISTICAL REPORTS
  • INTRODUCTION TO CLINICAL STUDY REPORT (CSR)
  • SAS PROGRAMS DEVELOPMENT AND VALIDATION (QC)
  • MeDRA GUIDELINES
  • GENERATING SUMMARY REPORTS
  • GENERATING LISTINGS
  • GENERATING GRAPHS
  • REAL TIME PROJECT ON PHASE II CLINICAL TRIAL STUDIES (ONCOLOGY & DIABETES THERAPEUTIC AREA)

Module 5: DEFINE.XML

  • INTRODUCTION TO DEFINE.XML
  • INTRODUCTION TO OPEN CDISC

Module 6: PINNACLE 21

  • HOW TO USE P21 TOOL
  • HOW TO CHECK AND RESOLVE P21 ISSUE

Module 7: SUBMISSION DOCUMENTS

  • SDRG (STUDY DATA REVIEWER’S GUIDE)
  • ADRG (ANALYSIS DATA REVIEWER’S GUIDE)

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