Efficiently Transforming Clinical Data Collected With InForm™ into SDTM Format

Wednesday, 13 May 2009, 13:00 – 16:00

Many companies are planning to electronically submit clinical data to regulatory agencies and want to utilise CDISC standards to transform their clinical data into SDTM format. The SDTM transformation process, however, can be time-consuming and costly without the necessary preparation and familiarity with current standards.

During this session, you will be provided with a brief overview of current CDISC standards; with a focus on how to leverage CDASH based libraries and highlight potentially ambiguous areas within SDTM. The session speakers will discuss key challenges associated with transforming clinical data collected with InForm into STDM format and provide recommendations to help your organisation make this process more accurate and efficient.

Also reviewed, will be how the FDA views your clinical data using WebSDM™ and how to check and review your clinical data through the course of the entire study.

Workshop Leader:
Robert Quinn, Manager, Product Marketing

To register for the conference
To view our preliminary agenda