SDTM ADaM Implementation FAQ

Project Scope 

The Standards Implementation Nuances sessions at the March North America 2016 CSS and June EU 2016 CSS surfaced various common challenges amongst SDTM and ADaM implementers and consumers. In addition, there were many questions discussed related to data submissions requirements by various regulatory agencies around the world (e.g. FDA, PMDA, NMPA). It became very clear that the Industry is in need of a forum and subsequent knowledge-base (FAQ) to address these challenges. This project team was formed in June 2016 to collaborate with Subject Matter Experts (SMEs) from the industry, CDISC, and the FDA. The goal of this project team is to:

  1. Collect frequently asked questions (FAQs) from Industry. If you have a question for the team, email workinggroups@phuse.global.

  2. Assess the appropriateness of a question, develop & review a response, collaborate with CDISC/FDA for clarity if required.

  3. Publish the FAQ and responses on Advance Hub database for helpful implementation/strategy information.

Project LeadsEmail
Aatiya Zaidi, Gileadaatiya.zaidi@gilead.com
Amy Palmer

TBC

Bhavin Busa, Clymb Clinical bhavin@clymbclinical.com
Nicola Newton, PHUSE Project Assistant

nicky@phuse.global

CURRENT STATUS Q4 2024

  • No update.
Objectives & Deliverables Timelines 

Publish responses to questions received under: 

Ongoing 

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