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Webinar -   How To Accelerate & Improve the Quality of CDISC SDTM Deliverables: Design with the End in Mind
Webinar -   How To Accelerate & Improve the Quality of CDISC SDTM Deliverables: Design with the End in Mind
Webinar
Online

Webinar - How To Accelerate & Improve the Quality of CDISC SDTM Deliverables: Design with the End in Mind

By

XTalks

1 Followers
30 Nov -0001
Free Registration

Event Details

Webinar - How To Accelerate & Improve the Quality of CDISC SDTM Deliverables: Design with the End in Mind

Since the FDA passed regulations requiring submitted datasets to be compliant with the CDISC Study Data Tabulation Model (SDTM), clinical trial sponsors have faced a dilemma. Should they design electronic case report forms (eCRFs) in line with SDTM from the outset? Or should they retrospectively convert data to CDISC SDTM at the end?

A retrospective approach is fraught with risk. What if some of the required data is missing? Will it be possible to retrofit datasets and terminology into the CDISC SDTM and NCI Controlled Terminology models? Will the submission be compliant?

This time-consuming data wrangling distracts resources from the important business of delivering a high quality submission package – before the deadline!

Register for this webinar and hear from leading industry experts about designing studies with the end in mind — and how technology can be leveraged to facilitate this.

Entry Fees

Free Registration

Categories

Event Frequency

One Time

Event Timings

(GMT-7:00) Vancouver
01:00 PM - 02:00 PM (Dec 01) (General)

Organizer

XTalks

1 Followers

Always at the forefront of digital media, we strive to connect practitioners with quality content in the most accessible and interactive way possible. Our online communities serve as knowledge hubs and information exchanges, enabling industry prof...

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