Learn from standards experts during our monthly webinars.

 

Access to past webinars can be found at the bottom of this page.

CDISC Public Webinar Series - Standards Updates and Additions

13 Oct 2016

10:00-11:30 AM CST

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Agenda

  • Ebola TA Public Review
  • Malaria TA Public Review

Panelists

  • Maura Kush, CDISC Specialist and Data Standards Consultant, Pharmastat
  • Shannon Labout CCDM, Vice President of Education, CDISC
  • Bess LeRoy, Metadata Engineer, CDISC
  • Diane Wold, Senior Director, Standards Development and Modeling, CDISC

CDISC Members Only Mini-Training Series - Some Considerations When Designing ADaM Datasets

9 MAR 2017

10:00-11:30 AM CST

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Please register for this members only webinar using your organizational e-mail address. If you aren't sure whether your organization is a CDISC Member, please review the member list here and confirm before you register. Thank you.

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Description
The ADaMIG has many variables defined and recommendations on creating user-defined variables. What actually makes sense on a study level can sometimes be difficult to determine. Some of the presenter’s experiences and suggestions will be shown to help clarify what should and should not be done when creating ADaM dataset designs.

Panelist

Nate Freimark, Vice President - Clinical Programming and Date Standards, The Griesser Group

CDISC Members Only Mini-Training Series - Deconstructing ADRS: Tumor Response Analysis Data Set

12 Jan 2017

10:00-11:30 AM CST

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Please register for this members only webinar using your organizational e-mail address. If you aren't sure whether your organization is a CDISC Member, please review the member list here and confirm before you register. Thank you.

 

Click here to ensure your machine has the necessary requirements to run CDISC webinars (run by Citrix).

Title:

CDISC Members Only Mini-Training Series - Deconstructing ADRS: Tumor Response Analysis Data Set

 

Description:

From the perspective of someone new to both the oncology therapy area and ADaM, this presentation describes the experience of working with an already-existing data set used for the analysis of tumor responses. Progressively detailed analysis needs of a protocol are explained along with their impact on the design of the ADaM data set, in terms of structure and derived parameters. No prior knowledge of oncology studies or tumor data domains is necessary, as concepts will be explained throughout and the focus will be on the ADaM implementation and lessons learned. 

Agenda: 
• Deconstructing ADRS: Tumor Response Analysis Data Set 

Presenter: 
• Steve Almond, Lead Statistical Analyst, Bayer 

Q&A Panelists: 
• Nate Freimark, Senior Director of the Biometrics Operations Standards Group, Theorem Clinical Research 
• Susan Kenny, President, Maximum Likelihood 
• Mario Widel, Research Scientist, Eli Lilly and Company

CDISC Tech Webinar Series - TRANSFoRm Project, Biomedical Concepts, SHARE and the Semantic Web

Nov 10 2016

10:00-11:30 AM CST

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  • TRANSFoRm Project: ODM-XML Extension in User Interface for Mobile Apps
    • Agenda
      • ODM-XML integration in generating mobile applications 
    • Panelists
      • Vasa Curcin, Lecturer in Health Informatics, King’s College London 
      • Stanisław Saganowski, Wrocław University of Science and Technology, Poland, Research Assistant
      • Piotr Bródka, Wrocław University of Science and Technology, Poland, Assistant Professor
      • Radosław Michalski, Wrocław University of Science and Technology, Poland, Assistant Professor
      • Brendan Delaney, TRANSFoRm Project 
  • Biomedical Concepts, SHARE and the Semantic Web
    • Agenda
      • Managing new and existing studies that use different versions of the same standard and being able to update studies as new standards versions are released can be challenging. Without change control and the ability to understand how those changes will impact your systems, it becomes more difficult. This webinar will look at using Biomedical Concepts, SHARE content, the semantic web and tooling to facilitate standards implementation.
    • Panelists
      • Iberson-Hurst, CEO, Assero  

 

CDISC Members Only Mini-Training Series - Results Level Metadata: What, How and Why

16 Feb 2017

10:00-11:30 AM CST

Click here to register

Please register for this members only webinar using your organizational e-mail address. If you aren't sure whether your organization is a CDISC Member, please review the member list here and confirm before you register. Thank you.

Click here to ensure your machine has the necessary requirements to run CDISC webinars (run by Citrix).

 

Agenda

Results Level Metadata: What, How and Why 

Description

This webinar will provide an overview of results-level metadata – what it means, collection techniques, how it can be used during the creation of analysis displays,  and  what is needed for the define-xml to be results-level compliant. 

Panelists

• Frank DiIorio, President, CodeCrafters 

• Jeffrey Abolafia, Chief Strategist of Data Standards, Rho

CDISC Public Webinar Series - Standards Updates and Additions

20 Jun 2016

10:45 AM-12:15 PM CST

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Agenda

  • Diabetic Kidney Disease TA Public Review

Panelists

  • Rachael Zirkle, Lilly
  • Matthew Vitale, Lilly
  • Amy Mottl, University of North Carolina
  • Jordan Li, NCI-EVS
  • Gary Walker, Quintiles
  • Bess LeRoy, C-Path
  • Paula Martin, Independent Consultant

The World of Standards: CDISC and Beyond - Members Only Mini-Training Series

15 Dec 2016

10:00-11:30 AM CST

Click here to register

 

Please register for this members only webinar using your organizational e-mail address. If you aren't sure whether your organization is a CDISC Member, please review the member list here and confirm before you register. Thank you.

 

Click here to ensure your machine has the necessary requirements to run CDISC webinars (run by Citrix).

There are many standards available for defining safety and efficacy clinical trials data across industry, academia and government. Some are obvious, such as CDISC, but some are less well known. Some are required, others are highly recommended. Most provide existing materials that can jumpstart research, save time and money and provide numerous other benefits. This webinar:

  • Explores the definitions of "standards"
  • Reviews a wide range of data and process standards relevant to clinical research, including CDISC, initiatives at NIH, ISO standards, electronic health record initiatives and process improvement standards
  • Discusses the wider importance of using standards

Learning Outcomes:

  • Define the term “standards” in different contexts
  • Identify standards that are useful or required for various types of research
  • Select external standards that can benefit internal standards development and implementation

This webinar will benefit:

  • Heads and colleagues in:
  • Standards management
  • Process improvement
  • Clinical data management
  • EDC design and programming
  • CRF design
  • Database programming
  • Biostatistics
  • Clinical science/study management
  • Clinical Operations
  • People who are already familiar with the research landscape as well as those who are new to it

Panelist:

  • Kit Howard, Director of Education, CDISC