CDER/CBER s Top 7 CDISC Standards Issues
|
|
|
- Nelson Duane Norris
- 10 years ago
- Views:
Transcription
1 CDER/CBER s Top 7 CDISC Standards Issues Dhananjay Chhatre, MS, RAC edata Management Solutions Team Office of Business Informatics CDER, U.S. FDA Amy Malla Review Management CBER, U.S. FDA
2 Background ~ 30% of unique NDAs received by CDER in 2011 submitted CDISC/SDTM data ~ 20% of the BLA s received by CBER in 2011 submitted CDISC/SDTM data Although standardization has allowed for use of additional data analysis tools, issues with either the implementation of the standard, or the standard itself, have proven to be inhibitive to the regulatory review process
3 Top 6 Issues 1 Waste of Space 2 Extras 3 Validation Errors 4 Extended Codelists 5 ISO Dates 6 Traceability 7 Inadequate Documentation
4 1. Waste of Space edata team performed research on cause of large dataset sizes Randomly selected 20 studies (432 datasets) Identified correlation between dataset sizes and allotted column variable length Columns lengths were being padded i.e. actual length = 8, allotted length = 200 Impact on dataset size compounded by large number of rows
5 1. Waste of Space Reduced to the width needed Variable Name Variable Type Previous Variable Length Modified Variable Length DOMAIN Character 2 2 LBBLFL Character 2 2 LBCAT Character LBDTC Character LBNRIND Character 8 8 LBORNRHI Character LBORNRLO Character LBORRES Character LBORRESU Character LBREFID Character LBSEQ Numeric 8 8 LBSPID Character LBSTAT Character 8 8 LBSTNRHI Numeric 8 8 LBSTNRLO Numeric 8 8 LBSTRESC Character Totals bytes used ~ 1/10 the size LBSTRESN Numeric 8 8 LBSTRESU Character LBTEST Character LBTESTCD Character 8 8 STUDYID Character USUBJID Character VISIT Character VISITNUM Numeric 8 8 Total
6 1. Waste of Space Observed 70% file size reduction, on average, across 432 datasets Collaborated with Phrma group 14 participants (15 studies, 545 datasets) 68% file size reduction, on average But why is this phenomenon being seen in CDISC/SDTM datasets, and not legacy data?
7 1. Waste of Space SAS transport version 5 specifications allocate space within every row and column (cell) based on the overall column s defined variable length In the CDISC IG, an example references a column length of 200 It appears this example was taken to heart by industry Added wording in CDER Common Data Standards Issues Document and worked with CDISC to add similar wording in the recent update to clarify that column lengths should not be set to an arbitrary limit of 200 This requirement text will also be added to the Data Standards Specifications next revision (in progress)
8 2. Extras (Domains, Variables, SUPPQUAL) CDISC IGs (SDTM and ADaM) specify standard domains and variables, but allow sponsor to create their own domains and variables If no existing model seems appropriate SUPP- domains contain unnecessary information Use common sense and discuss with review team on whether all information in supp- datasets are necessary. For example, do not create a SUPPQUAL domain just to include the initials of the subject.
9 2. Extras (Domains, Variables, SUPPQUAL) The findings, events and interventions domain classes list variables that are allowable. Many of these variables are not in the published parent domain but instead placed in the SUPPQUAL. In compliance with the standard, the variables should be added to the parent domain and eliminated from SUPPQUAL If important variables (support key analyses) are placed in SUPPQUAL, discuss with the review team
10 3. Validation Errors CDER and CBER currently use OpenCDISC v1.2 Validation process results in error log -> read it! Errors and warnings that CAN be fixed, SHOULD be fixed Some errors/warnings will inherently exist because of your study design i.e. no baseline result, no exposure record Others won t Don t simply address and dismiss these errors in a Reviewer s Guide
11 3. Validation Errors Common Errors a) Codelist mis-match for extensible codelists b) End date is prior to start date c) Required and expected variables should be present in the dataset d) Variable labels in the dataset should match CDISC naming conventions e) AE set to serious but no qualifier exists that has been set to Y
12 4. Extended Codelists Submissions include codelists where variable values are not included in the codelist Incorrect define.xml
13 4. Extended Codelists Type Message N Rows Error Invalid ISO 8601 value 384 Informa The source data for SV is missing an 1 Warning Value for VSTEST not found in VSTEST 2840 Example of bad D efine.xml causing V S.T EST Codelist errors (CT 0054). < Item D e f OID ="VS.VSTEST CD " Nam e ="VSTESTC D " Da ta Type ="te x t " Leng th ="8 " O rig in =" A s s ign ed " Co m m e n t =" " de f : L a b el="vit a l Sig n s T e s t Sh o rt N a m e "> < C od elis t R ef Co d e L i s to I D =" VS_ VST EST C D _ C D "> < / C o de Lis t R e f > < d e f: V a lu e L is tr ef Va l u e L is t O ID ="VS. VS T E ST C D ~ Va l u e "> < / de f: V a lu e L is t R ef > </ Ite m D e f> < It em D e f OID ="VS.VSTEST " Nam e ="VSTEST " Da ta Type ="te x t " Le ng th =" 40 " O rig in =" A s s ign ed " Co m m e n t =" " de f : L a b el="vit a l Sig n s T e s t N a m e "> < C od elis t R ef Co d e L i s </ Ite m D e f> to I D =" VS_ VST EST _ C D " ></Co d e L i s tre f>
14 4. Extended Codelists Not in codelist 2/2/
15 4. Extended Codelists Fixed with one xml line edit 2/2/
16 5. ISO Dates SDTM IG allows for partial dates Date issues can arise from invalid ISO 8601 partial dates Start date and end date should contain similar length and characteristics Type Message N Rows Error Informati on Warning Invalid ISO 8601 value The source data for SV is missing an Value for VSTEST not found in VSTEST Common Problem
17 5. ISO Dates YYYY-MM-DDThh:mm:ss (i.e T07:10:15) Includes time element Only day (no time) Results in Invalid ISO 8601 value error Since time indicated in one column, standard time of midnight is assumed for 2nd, which occurs before start date, causing the error Clarification needs to occur in CDISC IGs regarding when to input times and when to omit If time was captured in CRFs, include in tabulations data Similar issue even when hour and minutes are captured (assumes seconds of :00 and triggers the error
18 6. Traceability No traceability between source data and datasets Need linkage: CRF -> SDTM -> ADaM -> CSR SDTM datasets should be created from CRFs If instead CRFs -> Raw -> SDTM, your analysis (and hopefully ADaM) datasets should be created from those same SDTM datasets, not the raw datasets Features exist in the ADaM standard that allow for traceability of analyses to ADaM to SDTM
19 6. Traceability CRF Creating SDTM and Analysis data from the raw data is incorrect (especially when submitting only SDTM and analysis data Raw data should create SDTM, and SDTM should then create Analysis Raw Data Analysis SDTM
20 7. Inadequate Documentation Often times not all aspects of the standard apply to your study/submission Submit supporting documentation in the form of a Reviewer s Guide to explain how the data standard was implemented: What is in the custom domains? What is in the suppqual s? Insufficient codelists? Unfixable errors/warnings and why? Derivation of key analysis variables
21 Contact Information: Please send CDER questions to: Please send CBER questions to: URLs: Study Data Standards for Submission to CDER ments/electronicsubmissions/ucm htm Study Data Standards for Submission to CBER htm Study Data Resources
USE CDISC SDTM AS A DATA MIDDLE-TIER TO STREAMLINE YOUR SAS INFRASTRUCTURE
USE CDISC SDTM AS A DATA MIDDLE-TIER TO STREAMLINE YOUR SAS INFRASTRUCTURE Kalyani Chilukuri, Clinovo, Sunnyvale CA WUSS 2011 Annual Conference October 2011 TABLE OF CONTENTS 1. ABSTRACT... 3 2. INTRODUCTION...
Lessons on the Metadata Approach. Dave Iberson- Hurst 9 th April 2014 CDISC Euro Interchange 2014
1 Lessons on the Metadata Approach Dave Iberson- Hurst 9 th April 2014 CDISC Euro Interchange 2014 2 Experience Human beings, who are almost unique in having the ability to learn from the experience of
SDTM AND ADaM: HANDS-ON SOLUTIONS
SDTM AND ADaM: HANDS-ON SOLUTIONS CDISC French Speaking User Group Paris, France 17 February 2012 Joris De Bondt, Head Data Standards & Process Improvements Tineke Callant, Senior Biostatistical Analyst
New features in SDTM-ETL v.1.2 1 SDTM-ETL TM. New Features in version 1.2
New features in SDTM-ETL v.1.2 1 SDTM-ETL TM New Features in version 1.2 This document describes the new features in version 1.2 of the SDTM-ETL TM software. It can be used in addition to the STDM-ETL
Training/Internship Brochure Advanced Clinical SAS Programming Full Time 6 months Program
Training/Internship Brochure Advanced Clinical SAS Programming Full Time 6 months Program Domain Clinical Data Sciences Private Limited 8-2-611/1/2, Road No 11, Banjara Hills, Hyderabad Andhra Pradesh
Implementation of SDTM in a pharma company with complete outsourcing strategy. Annamaria Muraro Helsinn Healthcare Lugano, Switzerland
Italian-Speaking CDISC User Group 2008 Implementation of SDTM in a pharma company with complete outsourcing strategy Annamaria Muraro Helsinn Healthcare Lugano, Switzerland Background Full outsourcing
Einführung in die CDISC Standards CDISC Standards around the World. Bron Kisler (CDISC) & Andrea Rauch DVMD Tagung 11.-14.
Einführung in die CDISC Standards CDISC Standards around the World Bron Kisler (CDISC) & Andrea Rauch DVMD Tagung 11.-14. März 2015 1 Outline Overview of CDISC Therapeutic Area Standards SHARE Metadata
A Macro to Create Data Definition Documents
A Macro to Create Data Definition Documents Aileen L. Yam, sanofi-aventis Inc., Bridgewater, NJ ABSTRACT Data Definition documents are one of the requirements for NDA submissions. This paper contains a
How to easily convert clinical data to CDISC SDTM
How to easily convert clinical data to CDISC SDTM Ale Gicqueau, Clinovo, Sunnyvale, CA Miki Huang, Clinovo, Sunnyvale, CA Stephen Chan, Clinovo, Sunnyvale, CA INTRODUCTION Sponsors are receiving clinical
Business & Decision Life Sciences What s new in ADaM
Business & Decision Life Sciences What s new in ADaM Gavin Winpenny 23 rd June 2015 Agenda What s happening CDISC and Regulatory Submission Landscape ADaM Implementation Guide ADaM Data Structures for
Bridging Statistical Analysis Plan and ADaM Datasets and Metadata for Submission
, October 24-26, 2012, San Francisco, USA Bridging Statistical Analysis Plan and ADaM Datasets and Metadata for Submission Abstract In this article, the relationship between the Statistical Analysis Plan
STUDY DATA TECHNICAL CONFORMANCE GUIDE
STUDY DATA TECHNICAL CONFORMANCE GUIDE Technical Specifications Document This Document is incorporated by reference into the following Guidance Document(s): Guidance for Industry Providing Regulatory Submissions
STUDY DATA TECHNICAL CONFORMANCE GUIDE
STUDY DATA TECHNICAL CONFORMANCE GUIDE Technical Specifications Document This Document is incorporated by reference into the following Guidance Document(s): Guidance for Industry Providing Regulatory Submissions
PharmaSUG2010 HW06. Insights into ADaM. Matthew Becker, PharmaNet, Cary, NC, United States
PharmaSUG2010 HW06 Insights into ADaM Matthew Becker, PharmaNet, Cary, NC, United States ABSTRACT ADaM (Analysis Dataset Model) is meant to describe the data attributes such as structure, content, and
Implementing the CDISC standards into an existing CDMS
Implementing the CDISC standards into an existing CDMS Presented by Ueng-Cheng Yang ([email protected]) Institute of Biomedical Informatics National Yang-Ming University 1 TCT is a resource center to support
Smart Dataset-XML Viewer: Web Services
Smart Dataset-XML Viewer: Web Services This version: 2015-01-25 Introduction We have developed some "RESTful" based webservices 1, and have implemented these, together with an already existing webservice
Use of standards: can we really be analysis ready?
Standards in analysis & reporting Use of standards: can we really be analysis ready? Analysis ready? Why? Reducing time to market/approval Reducing time to delivery Reducing re work Designing subsequent
A Brief Introduc/on to CDISC SDTM and Data Mapping
A Brief Introduc/on to CDISC SDTM and Data Mapping Agenda Flow of Clinical Trials Data The Problem Introducing CDISC Understanding SDTM Concepts of Data Mapping References 5/3/10 2 Flow of Clinical Trials
Copyright 2012, SAS Institute Inc. All rights reserved. VISUALIZATION OF STANDARD TLFS FOR CLINICAL TRIAL DATA ANALYSIS
VISUALIZATION OF STANDARD TLFS FOR CLINICAL TRIAL DATA ANALYSIS WENJUN BAO AND JASON CHEN JMP, SAS INC. PHUSE, SHANGHAI, NOV 28, 2014 OUTLINES: CDISC Standard SDTM ADaM Interactive Standardized TLFs Tables
Metadata Submission Guidelines Appendix to the Study Data Tabulation Model Implementation Guide
Metadata Submission Guidelines Appendix to the Study Data Tabulation Model Implementation Guide Prepared by the CDISC SDS Metadata Team Notes to Readers This is Version 0.9 of the Metadata Submissions
PharmaSUG2010 Paper CD04 CD04
CD04 The CDISC/FDA Integrated Data Pilot: A Final Summary of Findings, Reviewer Feedback, and Recommendations Implementing CDISC Standards Within and Across Studies Chris Decker, d-wise Technologies ABSTRACT
Using the SAS XML Mapper and ODS PDF to create a PDF representation of the define.xml (that can be printed)
Using the SAS XML Mapper and ODS PDF to create a PDF representation of the define.xml (that can be printed) Lex Jansen TAKE Solutions CDISC Atlantic User Group Meeting 2008-02-21 Regulatory Landscape (FDA)
ADaM Implications from the CDER Data Standards Common Issues and SDTM Amendment 1 Documents Sandra Minjoe, Octagon Research Solutions, Wayne, PA
ABSTRACT: ADaM Implications from the CDER Data Standards Common Issues and SDTM Amendment 1 Documents Sandra Minjoe, Octagon Research Solutions, Wayne, PA Over the past few years, the United States Food
PhUSE 2010. Paper CD13
Paper CD13 Clinical Data Interchange Standards Consortium (CDISC) integration into the Oracle Clinical/Remote Data Capture (OC/RDC) clinical data management system Peter Van Reusel, Business & Decision
How to build ADaM from SDTM: A real case study
PharmaSUG2010 - Paper CD06 How to build ADaM from SDTM: A real case study JIAN HUA (DANIEL) HUANG, FOREST LABORATORIES, NJ ABSTRACT: Building analysis data based on the ADaM model is highly recommended
STUDY DATA TECHNICAL CONFORMANCE GUIDE
STUDY DATA TECHNICAL CONFORMANCE GUIDE Technical Specifications Document This Document is incorporated by reference into the following Guidance Document(s): Guidance for Industry Providing Regulatory Submissions
PharmaSUG 2015 - Paper DS07
PharmaSUG 2015 - Paper DS07 The Best Practices of CDISC Validation Checks: Past, Present, and Future Shelley Dunn, d-wise, Morrisville, NC Ed Lombardi, Agility Clinical, Carlsbad, CA ABSTRACT The CDISC
The CDISC/FDA Integrated Data Pilot: A Case. Support an Integrated Review
The CDISC/FDA Integrated Data Pilot: A Case Studyin Implementing CDISC Standards to Support an Integrated Review d Wise Technologies Chris Decker Life Sciences Director Overview Pilot Mission and Goals
Managing Custom Data Standards in SAS Clinical Data Integration
PharmaSUG 2015 - Paper DS19-SAS Managing Custom Data Standards in SAS Clinical Data Integration ABSTRACT Melissa R. Martinez, SAS Institute, Inc., Round Rock, Texas, United States SAS Clinical Data Integration
SDTM-ETL TM. The user-friendly ODM SDTM Mapping software package. Transforming operational clinical data into SDTM datasets is not an easy process.
SDTM-ETL TM The user-friendly ODM SDTM Mapping software package Transforming operational clinical data into SDTM datasets is not an easy process. Therefore, XML4Pharma has developed a visual, easy-to-use
ABSTRACT On October 1st, 2008, CDASH released the first 16 common CRF streams (or domains) for use by the Pharmaceutical Industry.
Paper RS03-2008 A Practical Introduction to Clinical Data Acquisition Standards Harmonization (CDASH) Jennifer Price, Phoenix Data Systems, Inc, King of Prussia, PA ABSTRACT On October 1st, 2008, CDASH
Pharmaceutical Applications
Integrated Summary of Safety and Efficacy Programming for Studies Using Electronic Data Capture Changhong Shi, Merck & Co., Inc., Rahway, NJ Qing Xue, Merck & Co., Inc., Rahway, NJ ABSTRACT The Integrated
SDTM, ADaM and define.xml with OpenCDISC Matt Becker, PharmaNet/i3, Cary, NC
PharmaSUG 2012 - Paper HW07 SDTM, ADaM and define.xml with OpenCDISC Matt Becker, PharmaNet/i3, Cary, NC ABSTRACT Standards are an ongoing focus of the health care and life science industry. Common terms
Business & Decision Life Sciences CDISC Workshop: From SDTM to ADaM: Mapping Methodologies
Business & Decision Life Sciences CDISC Workshop: From SDTM to ADaM: Mapping Methodologies Jessica Minkue Mi Edou / 18th September 2014 From SDTM to ADaM: Mapping Methodologies CDISC and ADaM Introduc0on
Business & Decision Life Sciences
Business & Decision Life Sciences Define-it: Demo webinar Anne-Sophie Bekx / 20th May 2014 INSERT COMPANY LOGO IN MASTER SLIDE HERE History of Define.xml Define-it Software Demo Define-it versions Q &
Data Conversion to SDTM: What Sponsors Can Do to Facilitate the Process
Data Conversion to SDTM: What Sponsors Can Do to Facilitate the Process Fred Wood VP, Data Standards Consulting Octagon Research Solutions CDISC U.S. Interchange Baltimore, MD November 2009 1 Outline Background
Automate Data Integration Processes for Pharmaceutical Data Warehouse
Paper AD01 Automate Data Integration Processes for Pharmaceutical Data Warehouse Sandy Lei, Johnson & Johnson Pharmaceutical Research and Development, L.L.C, Titusville, NJ Kwang-Shi Shu, Johnson & Johnson
Common Misunderstandings about ADaM Implementation
PharmaSUG 2012 - Paper DS16 Common Misunderstandings about ADaM Implementation Nate Freimark, Theorem Clinical Research, King of Prussia, PA Susan Kenny, Amgen Inc, Thousand Oaks, CA Jack Shostak, Duke
Clinical Trial Data Integration: The Strategy, Benefits, and Logistics of Integrating Across a Compound
PharmaSUG 2014 - Paper AD21 Clinical Trial Data Integration: The Strategy, Benefits, and Logistics of Integrating Across a Compound ABSTRACT Natalie Reynolds, Eli Lilly and Company, Indianapolis, IN Keith
SDTM Validation: Methodologies and Tools
SDTM Validation: Methodologies and Tools Bay Area CDISC Implementation Network Meeting Friday, April 30 th, 2010 Dan Shiu Disclaimer The ideas and examples presented here do NOT imply: They have been or
Use of Metadata to Automate Data Flow and Reporting. Gregory Steffens Novartis PhUSE 13 June 2012
Use of Metadata to Automate Data Flow and Reporting Gregory Steffens Novartis PhUSE 13 June 2012 Stages of Metadata Evolution I In the beginning... No corporate or industry level data or reporting standards
Current Status and Future Perspectives for Systemization of Clinical Study related the issues of CDISC in USA and other
Current Status and Future Perspectives for Systemization of Clinical Study related the issues of CDISC in USA and other ABSTRACT The term "the CDISC standard" has been used incorrectly for a few years.
SDTM Validation Rules in XQuery
SDTM Validation Rules in XQuery FH-Prof. Dr. Jozef Aerts Univ. Appl. Sciences FH Joanneum Graz, Austria Can you understand the following validation rule (part 1)? SDTM Validation Rules in XQuery Jozef
Providing Regulatory Submissions In Electronic Format Standardized Study Data
Providing Regulatory Submissions In Electronic Format Standardized Study Data Guidance for Industry U.S. Department of Health and Human Services Food and Drug Administration Center for Drug Evaluation
ABSTRACT INTRODUCTION THE MAPPING FILE GENERAL INFORMATION
An Excel Framework to Convert Clinical Data to CDISC SDTM Leveraging SAS Technology Ale Gicqueau, Clinovo, Sunnyvale, CA Marc Desgrousilliers, Clinovo, Sunnyvale, CA ABSTRACT CDISC SDTM data is the standard
Robust tools to Create Define.xml v2.0 based submission components for SDTM, ADAM & SEND Vineet Jain, Independent Consultant
Robust tools to Create Define.xml v2.0 based submission components for SDTM, ADAM & SEND Vineet Jain, Independent Consultant In 2013 CDISC came out with define XML specification version 2.0. Unlike previous
Understanding CDISC Basics
Trends in Bio/Pharmaceutical Industry Understanding CDISC Basics Jane Ma Abstract Data standards can make data and its associated program more portable. The CDISC (Clinical Data Interchange Standards Consortium)
Vasanth Kumar Kunitala et al, SPJTS.1.(2),187-200 ISSN 2321-4597
BASIC USAGE OF CDISC SDTM GUIDANCE RULES TO STANDARDIZED DATASETSWITH SDTM DOMAINS VARIABLES AND VALUESAS PER FDA Vasanth Kumar Kunitala 1,Varun Kumar Sharma 2, Ikanshu Karla 3, Pradeep Moondra 4, Himansu
The ADaM Solutions to Non-endpoints Analyses
The ADaM Solutions to Non-endpoints Analyses ABSTRACT Chengxin Li, Boehringer Ingelheim Pharmaceuticals Inc., Ridgefield, CT, USA There always exist some analyses for non endpoints in the study. These
CREATING SV AND SE FIRST Henry B. Winsor, WinsorWorks, Limited, San Mateo, CA Mario Widel, Genentech, Inc., South San Francisco, CA
ABSTRACT PharmaSUG2010 - Paper CD09 CREATING SV AND SE FIRST Henry B. Winsor, WinsorWorks, Limited, San Mateo, CA Mario Widel, Genentech, Inc., South San Francisco, CA One current concern of the FDA is
CDISC Roadmap Outline: Further development and convergence of SDTM, ODM & Co
CDISC Roadmap Outline: Further development and convergence of SDTM, ODM & Co CDISC Ausblick: Weitere Entwicklung und Konvergenz der CDISC-Standards SDTM, ODM & Co. Jozef Aerts - XML4Pharma Disclaimer Views
Practical application of SAS Clinical Data Integration Server for conversion to SDTM data
Paper DM03 Practical application of SAS Clinical Data Integration Server for conversion to SDTM data Peter Van Reusel, Business & Decision Life Sciences, Brussels, Belgium Mark Lambrecht, SAS, Tervuren,
Analysis Data Model: Version 2.0
1 2 Analysis Data Model: Version 2.0 Prepared by the CDISC Analysis Dataset Modeling Team (ADaM) Notes to Readers This Model incorporates aspects of the previous General Considerations document version
ADaM or SDTM? A Comparison of Pooling Strategies for Integrated Analyses in the Age of CDISC
Paper CD01 ADaM or SDTM? A Comparison of Pooling Strategies for Integrated Analyses in the Age of CDISC Joerg Guettner, Bayer Pharma AG, Wuppertal, Germany Alexandru Cuza, UCB Biosciences GmbH, Monheim,
A white paper presented by: Barry Cohen Director, Clinical Data Strategies Octagon Research Solutions, Inc. Wayne, PA
THE CLINICAL DATA AND REGULATORY EXPERTS SDTM, Plus or Minus A white paper presented by: Barry Cohen Director, Clinical Data Strategies Octagon Research Solutions, Inc. Wayne, PA This Whitepaper is for
Sanofi-Aventis Experience Submitting SDTM & Janus Compliant Datasets* SDTM Validation Tools - Needs and Requirements
In-Depth Review of Tools to Check Compliance of CDISC - Ready Clinical s Bhavin Busa March 2 nd, 2011 Managing Clinical in the Age of CDISC BASUG Quarterly Meeting Presentation Outline Brief introduction
Metadata and ADaM. www.cytel.com
Metadata and ADaM 1 Disclaimer Any views or opinions presented in this presentation are solely those of the author and do not necessarily represent those of the company. 2 Agenda Introduction of ADaM Metadata
Data Standards Strategy. Version: 1.0
Data Standards Strategy Version: 1.0 Document Date: December 5, 2012 Version Number REVISION HISTORY Implemented By Revision Date Description of Change 1.0 CDER DSPB December 5, 2012 Initial Document The
PharmaSUG2015 - Paper DS15
PharmaSUG2015 - Paper DS15 Considerations in Submitting Non-Standard Variables: Supplemental Qualifiers, Findings About, or a Custom Findings Domain Jerry Salyers, Accenture Accelerated R&D Services, Berwyn,
SAS CLINICAL TRAINING
SAS CLINICAL TRAINING Presented By 3S Business Corporation Inc www.3sbc.com Call us at : 281-823-9222 Mail us at : [email protected] Table of Contents S.No TOPICS 1 Introduction to Clinical Trials 2 Introduction
SDTM-ETL 3.1 New Features
SDTM-ETL 3.1 New Features SDTM-ETL 3.1 has a lot of new features. The most important ones are listed and explained in this document which lists all major new features of versions 3.0 and 3.1. Support for
Guidance for Industry
Reprinted from FDA s website by EAS Consulting Group, LLC Guidance for Industry Providing Regulatory Submissions in Electronic Format Standardized Study Data DRAFT GUIDANCE This guidance document is being
Strategies and Practical Considerations for Creating CDISC SDTM Domain Data Sets from Existing CDM Data Sets
Paper FC05 Strategies and Practical Considerations for Creating CDISC SDTM Domain Data Sets from Existing CDM Data Sets Robert W. Graebner, Quintiles, Inc., Overland Park, KS ABSTRACT Creating CDISC SDTM
Analysis Data Model (ADaM)
Analysis Data Model (ADaM) Prepared by the CDISC Analysis Data Model Team Notes to Readers This is Version 2.1 of the Analysis Data Model (ADaM) Document. It includes modifications so that it corresponds
CDISC standards and data management The essential elements for Advanced Review with Electronic Data
Session 6: Toward Electronic Submission of Study Data for New Drug Applications CDISC standards and data management The essential elements for Advanced Review with Electronic Data Yuki Ando Senior Scientist
Trials and Tribulations of SDTM Trial Design
PharmaSUG 2011 - Paper CD13 Trials and Tribulations of SDTM Trial Design Fred Wood, Octagon Research Solutions, Wayne, PA Mary Lenzen, Octagon Research Solutions, Wayne, PA ABSTRACT An increasing number
CDISC Asthma Therapeutic Area Data Standards User Guide Yes, it is interesting! Paul Terrill
CDISC Asthma Therapeutic Area Data Standards User Guide Yes, it is interesting! Paul Terrill Rather dry no statistics here Standards matter Must have been a lot of hard work! 2 What I am not going to talk
PharmaSUG 2015 Paper SS10-SAS
ABSTRACT PharmaSUG 2015 Paper SS10-SAS Using SAS Clinical Data Integration to Roundtrip a Complete Study Study Metadata (Define-XML) and Study Data (Dataset-XML) Ken Ellis, SAS Institute Inc., Cary, NC,
PK IN DRUG DEVELOPMENT. CDISC management of PK data. Matteo Rossini Milan, 9 February 2010
Matteo Rossini Milan, 9 February 2010 Introduction to CDISC CDISC: Clinical Data Interchange Standards Consortium CDISC is a global, open, multidisciplinary, non-profit organization that has established
ProjectTrackIt: Automate your project using SAS
Paper PP09 ProjectTrackIt: Automate your project using SAS Abhishek Bakshi, Cytel, Pune, India ABSTRACT Entering information in a project programming tracker is one of the menial tasks taking up time which
Analysis Data Model (ADaM) Implementation Guide
Analysis Data Model (ADaM) Implementation Guide Prepared by the CDISC Analysis Data Model Team Notes to Readers This Implementation Guide is Version 1.0 (V1.0) and corresponds to Version 2.1 of the CDISC
Using SAS Data Integration Studio to Convert Clinical Trials Data to the CDISC SDTM Standard Barry R. Cohen, Octagon Research Solutions, Wayne, PA
Using SAS Data Integration Studio to Convert Clinical Trials Data to the CDISC SDTM Standard Barry R. Cohen, Octagon Research Solutions, Wayne, PA ABSTRACT A new industry standard for clinical trials data,
Alcohol Use Disorder Identification Test Self-Report Version (AUDIT-SR)
Alcohol Use Disorder Identification Test Self-Report Version (AUDIT-SR) Questionnaire Supplement to the Study Data Tabulation Model Implementation Guide for Human Clinical Trials Prepared by TBI Standards
Building and Customizing a CDISC Compliance and Data Quality Application Wayne Zhong, Accretion Softworks, Chester Springs, PA
WUSS2015 Paper 84 Building and Customizing a CDISC Compliance and Data Quality Application Wayne Zhong, Accretion Softworks, Chester Springs, PA ABSTRACT Creating your own SAS application to perform CDISC
Clinical Data Management (Process and practical guide) Dr Nguyen Thi My Huong WHO/RHR/RCP/SIS
Clinical Data Management (Process and practical guide) Dr Nguyen Thi My Huong WHO/RHR/RCP/SIS Training Course in Sexual and Reproductive Health Research Geneva 2012 OUTLINE Clinical Data Management CDM
Overview of CDISC Implementation at PMDA. Yuki Ando Senior Scientist for Biostatistics Pharmaceuticals and Medical Devices Agency (PMDA)
Overview of CDISC Implementation at PMDA Yuki Ando Senior Scientist for Biostatistics Pharmaceuticals and Medical Devices Agency (PMDA) CDISC 2012 Outline Introduction Update of PMDA activity CDISC implementation
Synergizing global best practices in the CRO industry
Synergizing global best practices in the CRO industry KREARA - India Established on April 24 th 2004 Contract Research Services to Pharmaceutical companies Clinical Data management and Biometrics Interactive
Package R4CDISC. September 5, 2015
Type Package Title Read CDISC Data Files Version 0.4 Date 2015-9-5 Depends R (>= 3.0.3, XML Author Package R4CDISC September 5, 2015 Maintainer URL https://github.com/i-akiya/r4cdisc
Implementing CDASH Standards Into Data Collection and Database Design. Robert Stemplinger ICON Clinical Research
Implementing CDASH Standards Into Data Collection and Database Design Robert Stemplinger ICON Clinical Research 1 Agenda Reasons for Using CDASH Project Outline Implementation Discussion of Results Reasons
Note: See 7.7 Representations and Warranties, Limitations of Liability, and Disclaimer.
Clinical Data Acquisition Standards Harmonization (CDASH) Prepared by: CDISC and Domain Teams CDASH_STD-1.0 01/OCT/2008 CDASH V1.0 STANDARD Revision History Document Number Release Date Updates CDASH_STD-1.0
Did you know? Accenture can deliver business outcome-focused results for your life sciences research & development organization like these:
How can Accenture Accelerated R&D BPO Services help you achieve greater business value? Did you know? Accenture can deliver business outcome-focused results for your life sciences research & development
The CDISC Study Data Tabulation Model (SDTM): History, Perspective, and Basics Fred Wood Principal Consultant, Octagon Research Solutions
Paper RS10 The CDISC Study Data Tabulation Model (SDTM): History, Perspective, and Basics Fred Wood Principal Consultant, Octagon Research Solutions ABSTRACT The CDISC (Clinical Data Interchange Standards
SAS CLINICAL STANDARDS TOOKIT
You can read the recommendations in the user guide, the technical guide or the installation guide for SAS CLINICAL STANDARDS TOOKIT 1.3. You'll find the answers to all your questions on the SAS CLINICAL
How to Use SDTM Definition and ADaM Specifications Documents. to Facilitate SAS Programming
How to Use SDTM Definition and ADaM Specifications Documents to Facilitate SAS Programming Yan Liu Sanofi Pasteur ABSTRCT SDTM and ADaM implementation guides set strict requirements for SDTM and ADaM variable
Guidance for Industry
Guidance for Industry Cancer Drug and Biological Products Clinical Data in Marketing Applications U.S. Department of Health and Human Services Food and Drug Administration Center for Drug Evaluation and
Clinical Data Acquisition Standards Harmonization: Basic Data Collection Fields for Case Report Forms
Clinical Data Acquisition Standards Harmonization: Basic Data Collection Fields for Case Report Forms Prepared by the CDISC CDASH Team Notice to Reviewers This is the CDASH draft posted for public comment.
WHITE PAPER. CONVERTING SDTM DATA TO ADaM DATA AND CREATING SUBMISSION READY SAFETY TABLES AND LISTINGS. SUCCESSFUL TRIALS THROUGH PROVEN SOLUTIONS
WHITE PAPER CONVERTING SDTM DATA TO ADaM DATA AND CREATING SUBMISSION READY SAFETY TABLES AND LISTINGS. An innovative approach to deliver statistical analysis and data in a CDISC ADaM complient manner
ABSTRACT INTRODUCTION PATIENT PROFILES SESUG 2012. Paper PH-07
Paper PH-07 Developing a Complete Picture of Patient Safety in Clinical Trials Richard C. Zink, JMP Life Sciences, SAS Institute, Cary, NC, United States Russell D. Wolfinger, JMP Life Sciences, SAS Institute,
CDISC Journal. Regulatory Submissions for Medical Devices and Diagnostics: The Basics
CDISC Journal Clinical Data Interchange Standards Consortium O ctober 2011 Regulatory Submissions for Medical Devices and Diagnostics: The Basics By Carey G. Smoak Abstract Medical devices and diagnostics
Udo Siegmann member of e3c, CDISC Sen. Dir. Acc. Management PAREXEL
Innovative Medicines Technological Platform Udo Siegmann member of e3c, CDISC Sen. Dir. Acc. Management PAREXEL Facts about PAREXEL Full service CRO (Clinical Research Organisation) Involved in more than
Guidelines on the Nonconformity Grading and Exchange Form MDSAP AU G0019.4.002
Guidelines on the Nonconformity Grading and Exchange Form MDSAP AU G0019.4.002 Purpose This guidance document explains the features of the Excel Form MDSAP AU F0019.2 - MDSAP Nonconformity Grading and
Janus Clinical Trials Repository (CTR) An Update
Janus Clinical Trials Repository (CTR) An Update Armando Oliva, M.D. Associate Director for Informatics CDER Office of Computational Science U.S. Food and Drug Administration 2015-03-16 The views expressed
CDISC SDTM/ADaM Pilot Project 1 Project Report
Executive Summary Background CDISC SDTM/ADaM Pilot Project 1 Project Report CDISC is a non-profit, multidisciplinary consensus based standards development organization founded over a decade ago that has
UTILIZING CDISC STANDARDS TO DRIVE EFFICIENCIES WITH OPENCLINICA Mark Wheeldon CEO, Formedix Boston June 21, 2013
UTILIZING CDISC STANDARDS TO DRIVE EFFICIENCIES WITH OPENCLINICA Mark Wheeldon CEO, Formedix Boston June 21, 2013 AGENDA Introduction Real World Uses : Saving Time & Money. Your Clinical Trials Automated.
PhUSE Annual Meeting, London 2014
PhUSE Annual Meeting, London 2014 Metadata, Study data standards, Master data, terminology, interoperability: Key concepts underlying compliance to FDA guidance on electronic submission Isabelle de Zegher,
Development of CDISC Tuberculosis Data Standards
Development of CDISC Tuberculosis Data Standards Michael Fiola Senior Director / Quintiles The presenters have disclosed that they have no proprietary or financial interests in the topics covered in this
Electronic Submission of Regulatory Information, and Creating an Electronic Platform for Enhanced Information Management
Written Notice of Participation by the Clinical Data Interchange Standards Consortium (CDISC) and Written Statement for Discussion Topics to be Addressed In the FDA Public Hearing: Electronic Submission
