Study Data Reviewer's Guide

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Revision as of 00:29, 3 November 2012 by ScottBahlavooni (talk | contribs) (SDRG Deliverables)
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Overview & Scope

CGD-010: define.XML does not adequately document SDTM mapping decisions, sponsor-defined domains, sponsor-defined controlled terminology, and sponsor extensions to CDISC controlled terminology. A standardized Data Guide would help to address this documentation gap. The content of the Data Guide should be standardized and developed jointly between CDER, Industry, and CDISC.

Scope: The Study Data Reviewer's Guide (SDRG) will be proposed as a component of the eCTD's Module 5 SDTM data documentation.  This document will be defined for SDTM data descriptions only. An Analysis Data Reviewer's Guide will be handled in a future project.

SDRG Core Team

Helena Sviglin, FDA
Douglas Warfield, FDA
Gail Stoner, J&J
Joanna Koft, Biogen Idec
Scott Bahlavooni, Genentech
John Brega, Pharmastat

SDRG Deliverables

SDRG Completion Instructions (Draft posted 02-Nov-2012)
SDRG Template
SDRG Examples

SDRG Project Plan

SDRG Completion Instructions first draft: 29Oct2012 - 02Nov2012
SDRG Template first draft: 29Oct2012 - 15Nov2012
Pre-qualification of SDRG Instructions: 05Nov2012 - 30Nov2012
Compile findings from pre-qualification and finalize SDRG Instructions and Template: 01Dec2012 - 15Dec2012
Identify data for development of SDRG Examples including authorization from sponsor companies to permit the use of "dummied" references to corporate data in examples: 29Oct2012 - 15Dec2012
SDRG Examples: 01Jan2013 - 30Jan2013
WG4 Review of SDRG Deliverable Package 31Jan2013 - 28Feb2013

Archived Content

Data Guide - An Analysis, FDA Template, Examples
Data Guide Development - Study Level
Data Guide Development - Data Description
Data Guide Devlopment - Data Validation

Keep it small, keep it simple, keep it moving