Metadata Usage in Clinical Trials
The 23rd May saw the 3rd PHUSE UK Single Day Event at the spacious Astra Zeneca offices in Granta Park, Cambridge.The event was attended by over 80 European delegates across 40 companies.
The speakers from industry took to the podium one by one to explore Metadata in Clinical Trials from a number of perspectives. From MDR's (Metadata data Repository), to using Metadata to visualise data, to using metadata to auto generate SDTM's, ADAM's, Tables, figures and Listings.
Over lunch and during the networking breaks delegates were free to carry on with the dialogue generated from the sessions, making new allies across the various sections of our industry.
With the encouraging feedback that we received it looks like we can plan for another UK SDE in 2017!
CDISC Standards: Can the Semantic Web Help? - David Iberson-Hurst, Assero
Confirming MDR Metadata Requirements for Operational Implementation - Andy Richardson, d-Wise
Effective and Operational Use of CDISC Standards and Study Metadata Embedded in SAS Life Science Analytics Framework - Stijn Rogiers, SAS
Why Modern CDISC Data Visualisation Matters in Clinical Trials - Valérie Nedbal, JMP
NO SLIDES WILL BE AVAILABLE FOR THIS PRESENTATION
Metadata-driven, Standards-based Clinical Analysis and Reporting Environment - Alex Hromcenco & Tony Allen, AstraZeneca
Metadata-driven SDTM Creation: A Human Perspective - Edward Jones, PRA
Using Metadata to Create Table-producing SAS® Programs at Amgen Inc - Neil Lyon, Amgen
Download the Brochure Here
Photos from the day