Difference between revisions of "CTRR Working Documents"
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===Storyboards=== | ===Storyboards=== | ||
Revision as of 21:17, 28 January 2010
Return to CTRR main page
Contents
- 1 Current Working Documents
- 2 Existing Artifacts relevant to the Project
- 2.1 CTSA (Clinical Translational Science Award)
- 2.2 CONSORT
- 2.3 CONSORT Mapping - CDISC
- 2.4 ClinicalTrials.gov
- 2.5 EMEA - EudraCT
- 2.6 WHO
- 2.7 Protocol Representation – CDISC
- 2.8 CDISC-HL7 Study Participation Message
- 2.9 CDISC-HL7 Study Design Message
- 2.10 CDISC-HL7 Study Data Message
- 2.11 BRIDG Model
- 2.12 CDISC ADAM
- 2.13 SAP – Statistical Analysis Plan
- 2.14 HL7 - Detailed Clinical Model (DCM)
- 2.15 EHR project
- 2.16 Public Health Emergency Response (PHER)
- 2.17 Mapping Protocol terms to MeSH
- 2.18 American Immunization Registry Association (AIRA) – Pediatric messages for immunizations
- 2.19 Other “older” organization registries, ie, American College of Cardiology
Current Working Documents
EudraCT Mapping Documents
- 2010-Jan14 Meeting Minutes
Storyboards
Previous versions removed... .
Activity, Interaction and Trigger Events Diagrams
CTRR Activity, Interaction and Trigger Events Model - PPT
Other Documents
CTRR Enterprise Architect - EAP
.
Existing Artifacts relevant to the Project
CTSA (Clinical Translational Science Award)
Informatics : Use Cases for the CTSA Human Studies Database project
CONSORT
CONSORT - Transparent Reporting of Trials Home Page
The CONSORT statement (Consolidated Standards of Reporting Trials)
A template of the CONSORT checklist
CONSORT Mapping - CDISC
WHO Minimum trial Report to ICH E3 and CDISC Protocol Representation, CDISC SDTM (in BRIDG Model)
Comparison and Rating of Clinical Trial Reporting Elements (ICH E3, CONSORT, WHO)
ClinicalTrials.gov
ClinicalTrials.gov Protocol Data Element Definitions (DRAFT) as 2/5/2009
ClinicalTrials.gov Protocol Data Element Definitions (Direct Link)
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ClinicalTrials.gov Basic Results - Data Element Definitions (DRAFT) as 2/5/2009
ClinicalTrials.gov Basic Results - Data Element Definitions (Direct Link)
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.
EMEA - EudraCT
.
WHO
WHO Trial Registration Data Set Version 1.0
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Protocol Representation – CDISC
Protocol Elements for Regulated Clinical Trials
.
CDISC-HL7 Study Participation Message
Study Participation Domain Analysis Model
CDISC-HL7 Study Design Message
CDISC-HL7 Study Data Message
Unavailable at this time
BRIDG Model
clinicaltrials.gov mapping document to BRIDG 2.1
CDISC ADAM
Final Release of Analysis Data Model Version 2.0
