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QRS

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ADAKIEP Composite Endpoint
ADaM ADSL
ADaM BDS of Changes in Weight and/or Body Mass Index (BMI)
ADaM BDS for average glucose measurements
ADaM BDS for time glucose measurements in range
ADaM Subject-level Analysis - ADSL Dataset
ADaM Basic Data Structure (BDS) using CRIT
ADaM Basic Data Structure (BDS) using PARAMCD
ADEXSUM Exposure
ADGFR Composite Endpoint
ADSL Endpoint
ADSL Composite Endpoint
Adverse Events (AE) with Device Event Reporting
All-cause Death
Analysis of Days Alive and Out of Hospital Composite Endpoint
Assay Kit and Properties
Background Heart Failure Maintenance Medications aCRF
Body Sites of Psoriasis Involvement at Baseline
Body Sites of Psoriasis Involvement at Baseline aCRF
Body Surface Area of Involvement (BSA)
Calculated Dose
Cardiac Surgery as an Acute Kidney Injury Risk Factor
CDASH. Device Exposure
CDASH. Device Identification
Concomitant Insulin Treatment 
Death
Death aCRF
Device Event Reporting 
Device Identification    
Device Setting that are Changeable   
Devices Used by Subjects to Manage Diabetes
Diabetes Complications aCRF
Diabetes Device Generated Messages or Alarms  
Diabetes Diagnosis
Diabetes History 1
Diabetes ADSL dataset
Diabetic Ketoacidosis Adverse Events
End-Stage Renal Disease
Example. Sequence Rearrangement Fusion
Example. Short Variation Insertions and Deletions
Example. Tumor Mutation Burden
Example. Variable Number of Tandem Repeats
Fixed Device Properties and Settings 
Glomerular Filtration Rate 1
Glomerular Filtration Rate 2
Heart Failure Background Maintenance Medications
Heart Failure Lab Tests
Heart Failure Medical History
Heart Failure Medical History aCRF
Historical Start Date of Menstruation
History of Menarche 
History of  Autoimmune Disease  (other than Diabetes) 
Hospitalization for Heart Failure
Hypoglycemia aCRF
Hypoglycemic Blood Glucose 1
Hypoglycemic Last Meal 1
Identification of Target Lesions and Measurements aCRF
Insulin Exposure  
Laboratory Results Collected for each Diabetic Ketoacidosis Event
Meal Tolerance Testing aCRF
Menarche During a Study 
On-Study Crohn's Disease Background Medication, Non-study Drugs
On-Study Crohn's Disease Background Medication, Non-study Drugs
Orchidometer Examination
Pancreatic Adenocarcinoma Cancer Genomic Findings
Pancreatic Cancer ADTTE Survival and Duration of Follow-up
Pancreatic Cancer Cachexia
Pancreatic Cancer Laboratory Findings 
Pancreatic Cancer Medical History aCRF
Pancreatic Cancer Pathology Report 
Pancreatic Cancer Primary Tumor Characteristics
Pancreatic Cancer Radiation Therapy aCRF
Pancreatic Cancer Radiation Therapy 
Pancreatic Cancer Stent Placement
Pancreatic Cancer Study Treatment Infusion aCRF
Pancreatic Cancer Study Treatment Infusion 
Pancreatic Cancer Surgical History
Pancreatic Cancer Surgical History aCRF
Pancreatic Cancer ADSL Dataset
Pancreatic Cancer Body Composition Measurements
Pancreatic Cancer Ki67 Microscopic Findings
Pancreatic Enzyme Replacement Therapy
Pancreatic Neuroendocrine Cancer Genomic Findings
Patient Global Impression
Phototherapy Administration
Plaque Psoriasis Medical History aCRF
Population PK - Multiple Subjects, Multiple Studies
Prior Crohn's Disease -Dependency on Corticosteroid Treatments
Prior Phototherapy
Prior Psoriasis Treatments aCRF
Proteinuria
Psoriasis Diagnosis
Renal Death 1
Renal Replacement Therapy
Renal Replacement Therapy 1
Renal Replacement Therapy aCRF
SDTM Prior Treatments and Vaccination History
Self-Monitoring Blood Glucose aCRF
Serum Creatinine and eGFR
Start Date of Menstruation During a Study 
Static Physician Global Assessment
Target Lesion Assessment
Testicular Volume
Tolerance Test 3
Transthoracic Echocardiography, MUGA Scan
Treatment Dispensed and Returned
Treatment Dispensed and Returned - Combination Drug
Tumor Specimen Collection and Handling 
Unplanned Healthcare Visits for Heart Failure 
Urine Protein 1
Urine Protein 2
Vaccination History aCRF
VAS for Itching and Quality of Life
 Diabetic Ketoacidosis - Device In-Use  At Time of Event 
 Diabetic Ketoacidosis Adverse Events
 Pancreatic Cancer Stent Placement aCRF

Event

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Event Date
PHUSE EU Connect 2022 -
PHUSE/FDA Computational Science Symposium (CSS) 2022 -
SCDM 2022 Annual Conference -
SCDM 2022 EMEA Conference -
PHUSE US Connect 2022 -
Controlled Terminology Updates for Q4 2021 -
PHUSE EU Connect -
PHUSE EU Connect -
2021 Japan Academic Workshop -
Controlled Terminology Updates for Q3 2021 -

Newsletter Article

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2021 TechniCon: Call for Applications
5th Italian CDISC User Group Annual Meeting
6th Annual Meeting of the CDISC Italian User Network: “What’s new at 360°
7th Annual Italian User Network Meeting
A Message from the CDISC Japan User Group
A PhUSE Perspective on the 2017 CDISC International Interchange
Accelerating drug development for Alzheimer's disease through the use of data standards
Achieving End-to-End Traceability Using Trace-XML
ADaM Conformance Rules v3.0 Released Fourth Quarter 2020
Announcing the CDISC Blue Ribbon Commissioners

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

Basic Page, Article

News

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CDISC and NORD Partner to Develop Data Standards for Rare Diseases
CDISC and One Mind Announce Availability of Research Data Standard for Traumatic Brain Injury
CDISC and OpenClinica Collaborate to Drive Academic Clinical Research Forward
CDISC and REDCap Work Together to Foster More Meaningful Clinical Research for Academics
CDISC and the Multi-Regional Clinical Trials Center of Brigham and Women’s Hospital (MRCT Center) collaborate to offer plain language clinical research definitions as a new standard
CDISC Founder to Lead ISO/TC215 Genomics Sub-Committee
CDISC is Proud to Announce a Research Collaboration to Incorporate FDA Business Rules into CDISC’s Open Rules Engine (CORE)
CDISC Launches Task Force to Rapidly Develop Standards for COVID-19
CDISC Names Chris Decker President and CEO
CDISC Names Dr. Maria Im Hee Shin Chair of Korea CDISC Coordinating Committee

Testimonials

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Quote
ADaM Primer

This is a good introduction to ADaM.
ADaM Theory and Application

The instructor not only has great knowledge and

ADaM Theory and Application

The instructor was excellent and extremely know

ADaM Theory and Application

It was very helpful to complete the exercises a

ADaM Theory and Application

The exercises were very useful and not too time

ADaM Theory and Application

The instructor was very interactive and was ver

ADaM Theory and Application

The extensive experience and the knowledge of t

ADaM Theory and Application

I am impressed by the instructor, she obviously

ADaM Theory and Application

It was a very interactive training with opportu

ADaM Theory and Application

The attendees shared a lot of their cases and a

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
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

Webinar

Therapeutic Area Version

Standard Version

Company

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Membership Level Company Address
Akebia Therapeutics Gold

245 First Street, Suite 1400
Cambridge, MA 02142
United States
Akros Pharma Inc Gold

United States
Alcedis GmbH Gold

Winchester Str. 3
35394 Giessen
Germany
Alcon Platinum

6201 South Freeway
Fort Worth, TX 76134
United States
Alimentiv, Inc. Platinum

100 Dundas Street Suite 200
London ON N6A 5B6
Canada
AliraHealth Gold

Route de Pré-Bois 14
1216 Geneva
Switzerland
ALK-Abello A/S Gold

Bøge Allé 6-8
Bygn. 10
2970 Hørsholm
Denmark
Almirall Gold

408-410 Barcelona Barcelona
Spain
Alnylam Pharmaceuticals Gold

300 Third Street
Cambridge, MA 02142
United States
AlphaLife Sciences Gold

Room 1515, Block B, 1188 Kaixuan North Road
Putuo Qu
Shanghai Shi, 200333
China

Courses

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Course Type
CDASH Course Public
CDASH Fundamentals and Implementation Online, Private, Public, Virtual Classroom
CDISC for Newcomers Private, Public
CDISC Library Workshop - Virtual
CDISC Open Rules Hands-on Implementation Training
CDISC Standards from the Start Public, Private
Common Sub-Domain Online
Constraints and Tags Online
Controlled Terminology Online, Private, Public, Virtual Classroom
Controlled Terminology Advanced Private, Public, Virtual Classroom

Instructors

Restricted

Displaying 1 - 40 of 40
2016 Europe Interchange Presentations
2016 International Interchange Presentations
2016 Japan Interchange Presentations
2017 China Interchange Presentations
2017 Europe Interchange Presentations
2017 International Interchange Presentations
2017 Japan Interchange Presentations
2018 China Interchange Presentations
2018 Europe Interchange Presentations
2018 Japan Interchange Presentations
2018 US Interchange Presentations
2019 China Interchange Presentations
2019 Europe Interchange Presentations
2019 Japan Interchange Presentations
2019 US Interchange Presentations
2019 US Interchange Presentations
2020 Europe Interchange Presentations
2020 Japan Interchange Presentations
2020 Technicon - Americas
2020 Technicon - Asia-Pacific
2020 Technicon - EMEA
2021 Technicon
CDISC 360
CDISC 360
CDISC Standards from the Start at ARO Council
CDISC/Microsoft Industry Stakeholder Workshop
Education - India Price Sheet for Online Courses
Education eBlast Host
Frankfurt 2017 Training Redirect
IntraChange 2017
President and Chief Executive Officer
QA Restricted
Send F2F
SHARE Exports (Safe)
Standards
Summer 2017 IntraChange
Test Redirect Link
Test Restricted
Test Vimeo - Static Embed
Working Group Meeting 2018

Team

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Published
Chainey Jonathan Blue Ribbon Commission Yes
Chou Sherry Blue Ribbon Commission Yes
Chow Anthony Blue Ribbon Commission Yes
Chronaki Catherine Board of Directors Yes
Curran Karen Board of Directors Yes
Decker Chris Executive Operations Yes
Franson Paul Blue Ribbon Commission Yes
Gersing Ken Blue Ribbon Commission Yes
Glover Hugh Blue Ribbon Commission Yes
Hardison David Board of Directors, Blue Ribbon Commission Yes
Structure Not Ready