Difference between revisions of "Analysis Data Reviewer's Guide"

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|Susan Kenny||Industry Co-Lead||Amgen||susan.kenny@amgen.com
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|Gail Stoner||Industry Co-Lead||Johnson & Johnson||GStoner@its.jnj.com
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|Mina Hohlen||FDA Observer||FDA||mina.hohlen@fda.hhs.gov
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Revision as of 12:45, 8 July 2013


Project Overview

ADaM “provides a framework that enables analysis of the data, while at the same time allowing reviewers and other recipients of the data to have a clear understanding of the data’s lineage from collection to analysis to results. Although ADaM provides a robust metadata framework, FDA Reviewers benefit from additional, human-readable, documentation of analysis methods, datasets, and programs that cannot be fully explained within the ADaM metadata. The development of an Analysis Data Reviewer’s Guide (ADRG) template will ensure this documentation is provided to the agency in consistent and usable format.

Project Leads

Name Role Organization E-mail
Susan Kenny Industry Co-Lead Amgen susan.kenny (at) amgen.com
Gail Stoner Industry Co-Lead Johnson & Johnson GStoner (at) its.jnj.com
Mina Hohlen FDA Observer FDA mina.hohlen (at) fda.hhs.gov

Project Updates

Provide project updates in this section.

Objectives and Timelines

Objective Timeline
Determine the scope of the ADRG (e.g. analysis datasets, programs, overlap with SDRG) Complete during CSS
Develop draft ADRG template and completion instructions 2 months
Vet draft ADRG template and completion instructions 1 month
Finalize draft ADRG template and completion instructions and develop ADRG examples 3 months
Release ADRG work package for public comment 1 month
Finalize ADRG work package and release for use 1.5 months

Project Content and Activities

This section can document project activities or serve as a jumping off point to other pages in the project.

Meeting Minutes

ADRG Minutes 2013
CSS Meeting March 18-19, 2013

Archived Content