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$90.00

CDISC for Newcomers (Virtual)

Begins 15 Jul 2022
Available capacity: 30

Training Schedule Options (click on 'Read more...' to view all options)

The CDISC for Newcomers virtual training consists of contact hours (1 scheduled day of live Zoom instruction at 3 hours total). The CDISC Education Team will email all registered participants a Zoom link one week prior to the start of training.





See below for schedule options:













CDISC for Newcomers:
Region: Japan 日本
4 July
09:00 - 12:00 
Japan Standard Time (Japanese)

Region: China 中国
11 July
09:00 - 12:00
China Standard Time (Mandarin)

Region: India
15 July
14:00 - 17:00 
India Standard Time (English)





CDISC for Newcomers:
Region: US
6 September
09:00 - 12:00
US Eastern Time (English)


*Registration ends at 5:00pm EST (17:00) one business day prior to the training start date.

*Trainings will be rescheduled or cancelled if minimum enrollment requirements are not met.

Course Description

New to CDISC Standards? This 3-hour workshop will introduce the CDISC standards to help amplify the full potential of data, drive operational efficiencies, and expedite the regulatory review process. 

The workshop offers examples of the standards, along with how to build them into the process of writing a protocol, collecting and tabulating data, and using the data in analysis. 

The workshop also identifies standards strategies that can make the clinical research process more efficient and offers a high-level introduction into the current regulatory requirements for submissions.

The CDISC Data Exchange standards are reviewed, and the CDISC Library is discussed.

Agenda

  • Topic 1: What is CDISC?
  • Topic 2: Why Are Standards Needed?
  • Topic 3: Overview of Regulatory Requirements
  • Topic 4: Overview of CDISC Models
  • Topic 5: CDISC Connects Research Globally
  • Topic 6: Therapeutic Area User Guides
  • Topic 7: Data Exchange Standards
  • Topic 8: Implementing CDISC Standards
  • Topic 9: CDISC Library
  • Topic 10: How Does CDISC Work?

Learning Outcomes

  • Describe the CDISC Standards Development process, standards models, implementation guides and therapeutic area user guides to recognize their value in clinical research. 
  • Identify individual CDISC standards to set the stage for implementation. 
  • Support the adoption of implementing CDISC standards early in the clinical research process.
  • Interpret CDISC Therapeutic Area User Guides in order to implement them across foundational standards
  • Recognize how Define-XML organizes standards for as both machine-and human-readable metadata





Asia/Calcutta
Date: 15 Jul 2022
Start Time: 14:00
End Time: 17:00
Instructor : CDISC Authorized Instructor
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