Migration Summary - Content

	Event Date
CDISC 360: The Journey So Far and the Road Ahead	28 April 2020 - 28 April 2020
PHUSE Virtual Single Day Events	25 April 2020 - 31 December 2020
CDASH SAE Project	21 April 2020 - 21 April 2020
CDASH Office Hours	16 April 2020 - 16 April 2020
Controlled Terminology Updates for Q2	14 April 2020 - 14 April 2020
CDISC Initiatives Webinar	3 March 2020 - 3 March 2020
CDISC Strategic Plan: Clear Vision, Clear Impact	18 February 2020 - 18 February 2020
Public Review Webinar: Chinese Translations of SDTMIG v3.2, ADaMIG v1.1, ADaM OCCDS v1.0, ADaM v2.1	4 February 2020 - 4 February 2020
Public Training in Tokyo, Japan	27 January 2020 - 31 January 2020
Psoriasis Therapeutic Area User Guide Public Review	23 January 2020 - 23 January 2020

Newsletter Article

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CDISC Interchanges	Second Quarter 2019
CDISC Interchanges	Fourth Quarter 2019
CDISC Interchanges	Third Quarter 2019
CDISC Interchanges
CDISC Interchanges
CDISC International Interchange Brings Standards Community to Austin
CDISC is Evolving!
CDISC is Hiring!
CDISC is Hiring!
CDISC Japan Liaison Appointed	Second Quarter 2019

FAQ

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	FAQ Category
Does CDISC SHARE contain external non-CDISC standards like SNOMED, LOINC?	SHARE
Academic Integrity	Education
Another Community Question	Knowledge Base
Anti-Discrimination Policy	Education
Appropriate Student Behavior	Education
Are there QRS-like instruments for which the collected data would not be stored in the FT, QS, or RS domains?	QRS
CDISC Learner Records	Education
CDISC Learner Records	Education
General CEU Information	Education
General Course Costs and Payment Policies	Education
General Prerequisites	Education
I am interested in contributing to CDISC SHARE. How do I join?	SHARE
Learner Record Privacy and Information Security Policy	Education
Successfully Completing a Course	Education
What is included in a QRS Supplement?	QRS
What is the connection between CDISC SHARE and Controlled Terminology?	SHARE
What is the history of CDISC SHARE?	SHARE
What is the infrastructure that enables CDISC SHARE?	SHARE
Will companies be allowed to develop/add their custom elements and extend the Foundational Standards?	SHARE
Will I find electronic case report form (eCRF) vendor metadata in CDISC SHARE?	SHARE
With what standards does CDISC SHARE comply, beyond CDISC?	SHARE

Video

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Benefits of Membership and Volunteering	No
CDISC - Brand	No
CDISC’s Impact in Asia	No
Controlled Terminology	No
Impact for Academic Researchers	No
Introduction to ADaM	No
Introduction to SDTM Implementation Guide	No
Introduction to SEND Implementation Guide	No
Regulatory Requirements	No
TAUG	No
Traceability	No
What Are CDASH and the CDASH Model	No
What are SDTM and SDTM Concepts?	No
What is the CDASHIG?	No
Whiteboard	No

Basic Page, Article

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CDISCの新機能 - 患者財団

CDISCの新機能 - 規制機関

CFAST

China CDISC Coordinating Committee (C3C)

Clinical Trial Registration - Regulatory Compliance and Extending Beginning-to-End Data Quality for Clinical Trial

Colorbox Node Load

Controlled Terminology

Controlled Terminology Implementation

COVID-19 Interim User Guide Task Force

COVID-19 Therapeutic Area User Guide v2.0

News

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Testimonials

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News Link

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CDISC’s New Chief Standards Officer Looks To Improve Standards At “Inflection Point”

Improving Serious Adverse Event (SAE) Reporting In Clinical Trials

A Pragmatic Method for Transforming Clinical Research Data from the Research Electronic Data Capture “REDCap” to Clinical Data Interchange Standards Consortium (CDISC) Study Data Tabulation Model (SDTM): Development and Evaluation of REDCap2SDTM

A pragmatic tool for drug discovery

Accelerating drug development for Alzheimer's disease through the use of data standards

Achieving End-to-End Traceability

Alzheimer's treatments: What's on the horizon?

C-Path, CHDI and CDISC Announce Therapeutic Area User Guide for Huntington’s Disease

CDER Plots Pilot Project to Test CDISC Standard

CDISC launches COVID-19 research standards task force

CDISC Releases Data Management Guidance for COVID-19 Trials

CDISC US Interchange 2019 Keynote Address in Full

Clinical trials haven’t harnessed the digital revolution — TransCelerate’s latest initiative aims to change that

Clupea, KIT to establish Korea's 1st CDISC standard-based non-clinical big data platform

Cross-Stakeholder Collaboration: Advancing Research Through Common Protocol Templates

Data harmonisation for information fusion in digital healthcare: A state-of-the-art systematic review, meta-analysis and future research directions

Data Management Landscape is Still Changing, Are We Adapting Fast Enough?

Data Standards and ePRO Systems: A Road Less Travelled?

Data Standards in IDEA-FAST

EMA launches pilot project on analysis of raw data from clinical trials

End-to-end innovation in a regulated environment: applying spectral flow cytometry to clinical sample testing

FDA Binding Guidance: A Pivotal Milestone for CDISC Standards - Applied Clinical Trials

FHIR-to-CDISC Project Seeks to Facilitate Use of EHR Data in Clinical Research

Formedix and CDISC Join Forces to Provide Free Access to Ready-to-Use, CDASH-Compliant eCRFs for Accelerated Clinical Trial Set-Up

Harmonisation of large-scale, heterogeneous individual participant adverse event data from randomised trials of statin therapy

How Standardization Can Be An Innovation In Clinical Outsourcing

How TransCelerate, Microsoft, Accenture, and CDISC are Working to Revolutionize Digital Data Flow

Making Data Speak the Same Language

New CDISC Standards Make Sites’ AE Reporting Easier

Presenting and Sharing Clinical Data using the eTRIKS Standards Master Tree for tranSMART

SDTM vs CDASH: Why You Need Both!

Sharing and reuse of individual participant data from clinical trials: principles and recommendations

The CDISC Open Rules Engine (CORE): Open-Source Software For Clinical

The Turning Point for Clinical Research: Global Data Standardization

Therapeutic Area Data Standards for Autosomal Dominant Polycystic Kidney Disease: A Report From the Polycystic Kidney Disease Outcomes Consortium (PKDOC)

TMF Reference Model Affiliation With CDISC Could Improve TMF Interoperability

TransCelerate BioPharma & CDISC Collaborate on SAE Data Collection Standard

TransCelerate BioPharma Commences Collaborative Development of a Novel Digital Data Flow Solution for Study Start-Up

Use of CDISC Standards for Real-world Data: Expert Perspectives From a Qualitative Delphi Survey

Using a therapeutic area user guide to multiply research investments

Using Health IT Data Standards to Boost Interoperability for Clinical Research

Knowledge Base

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A Short History of CDISC and SAS Transport Files	Yes
Are These Findings Just Repeats or Were They Scheduled at Time Points?	Yes
Assessing Causality	Yes
Avoiding SDTM and ADaM Dataset and Variable Name Conflicts	Yes
Can I add this variable to my SDTMIG dataset?	Yes
CDISC ADaM Phases, Periods, and Subperiods: A Case Study	No
CDISC-Annotated CRF Repository in Japanese	Yes
Changing Event Severity	Yes
Concept Maps for a Finding with Increasing Levels of Detail	Yes
Concept Maps for Adverse Events with Increasing Levels of Detail	Yes
Concept Maps for Substance Administration with Increasing Levels of Detail	Yes
Considerations for Using CDISC Standards in Observational Studies	Yes
Controlled Terminology: FAQs	Yes
Country Coding	Yes
Do I have to use the variable labels in the SDTMIG?	Yes
Does QNAM Need to Start with a Domain Code?	Yes
Domain vs. Dataset: What's the Difference?	Yes
Domains are Topic-based, Except When They're Based on Structure	Yes
How Do I Represent a Pre-specified Finding?	Yes
How should I represent whether a physical exam was performed in SDTM?	Yes
Implementation of COVID-19 Pandemic Impact Standards	No
IS Domain Scope Update for the SDTMIG v3.4: A Development History and the Difficulties of Standardizing Complicated Biological Processes	Yes
LOINC and the SDTM	Yes
Making Clinical Data Acquisition Standards Harmonization (CDASH) Electronic Case Report Forms Available on the REDCap Shared Data Instrument Library	No
Making Sense of the Various ADaM Documents	Yes
Oncology Disease Response (RS) Supplements	Yes
Pre-specified Events and Pre-specified Findings	Yes
Providing Review-Ready Results in SDTM	Yes
QA Knowledge Base	No
SDTM and CDASH: Why You Need Both	Yes
SDTM Structure Diagrams	Yes
SDTM Timing Variables for Pre-study Findings	Yes
Sex and Gender	Yes
Special Values: "MULTIPLE" and "OTHER"	Yes
Standardized Lab Units	Yes
Study Subject Site Transfers Example	Yes
Study Subject vs. Experimental Unit	Yes
Subject Visits and COVID-19	Yes
TAUG Examples of SDTM Domains	Yes
Test Academic	No
Test Academic - Masquerade	No
The Magic that Happens between CDASH and SDTM	Yes
Translating CDASH "PRIOR" and "ONGO" to SDTM relative timing variables	Yes
UCUM and CDISC Codelists	Yes
Use of Fast Healthcare Interoperability Resources (FHIR) in the Generation of Real World Evidence (RWE)	Yes
Use of FHIR in Clinical Research: From Electronic Medical Records to Analysis	Yes
Use of HL7 FHIR as eSource to Pre-populate CDASH Case Report Forms using a CDISC ODM API	Yes
Variable Metadata Has Changed in SDTM v2.0. How Does This Affect SDTMIG v3.4?	Yes
What Do We Mean When We Say Provisional?	Yes
When Did That Happen? A Brief Guide to Representing Timing in SDTM.	Yes
When Would I Use ISO8601 Interval Format?	Yes
Where Does My Lab Data Go in SDTMIG v3.4?	Yes
Why Are Certain SDTM Variables "Not for Use in Human Clinical Trials"?	Yes
Why is an Image like a Specimen?	Yes
Why Not Just Use SNOMED?	Yes
Why Would a Standards Development Organization Make Non-standard Variables Available on their Website?	Yes

Resource

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Webinar

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Controlled Terminology Quarterly Update - Tuberculosis TA and COPD TA Public Review

Controlled Terminology Quarterly Update Q1 2015 and Medical Devices

Controlled Terminology Quarterly Update Q1 2016

Controlled Terminology Quarterly Update Q4 2015

Controlled Terminology Quarterly Updates Q1 2017

Controlled Terminology Quarterly Updates Q2 2016

Controlled Terminology Quarterly Updates Q2 2017

Controlled Terminology Update for Q1 - P57 Publication

Controlled Terminology Update for Q2 - P58 Public Review & CT Basics

Controlled Terminology Update Q2 2014

Therapeutic Area Version

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Standard Version

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Library of CDASH CRF Examples

Metadata Submission Guideline (MSG) for SDTMIG

Company

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	Membership Level	Company Address
CliniOps, Inc.	Gold	United States
Clinpharma Clinical Research LLC	Platinum	1000 N. West Street, STE 1200 Wilmington, DE 19801 United States
CLINSEARCH	Gold	110 AVENUE PIERRE BROSSOLETTE 92240 MALAKOFF France
Clinvia LLC	Gold	2500 Cary Regency Pkwy Cary, NC 27518 United States
CLUPEA Inc.	Platinum	United States
Clymb Clinical	Gold	49 Robinson Dr Bedford, MA 01730 United States
CMIC Holdings Co., Ltd.	Gold	Hamamatsucho Bldg, 1-1-1 shibaura Minato-ku, Tokyo 105-0023 Japan
Codex Scientific Co.,Ltd.	Gold	Room 318, Anda Building, No.1 Anyuan Road, Jingan Disctric, Shanghai Jing'an Qu Shanghai Shi, 210000 China
Cogent Biosciences	Gold	200 Cambridge Park Drive, Suite 2500 Cambridge , MA 02140 United States
Cognitive Research Corporation	Gold