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The scope of this project is to identify a primary and

back-up representative for each PHUSE regulatory referenced deliverable that will:

• review updates to regulatory documents where PHUSE deliverables are referenced to ensure they are in alignment

• identify any updates that are required due to updated regulatory documents

• organise the updates, including addressing feedback from PHUSE members

• discuss the updates with the ODS Working Group

• Leads to agree on the updates

• oversee the updates and publishing of PHUSE deliverables
• commit to serving as a representative for two years.

The project team will

meet quarterly with the ODS Working Group Leads to discuss potential updates and their timing to avoid burdening the project team members and

the regulatory authorities in reviewing the updated deliverables.

The Optimizing the Use of Data Standards Working Group is responsible for the maintenance of

four regulatory referenced deliverables (the cSDRG, ADRG, SDSP and BDRG) as well as three that will be published in the future. There is no regular maintenance process for updating these deliverables due to updates to binding and non-binding guidance from regulatory authorities. The project teams that were formed to create the documents no longer meet on a regular basis. This project will address the issue of implementing scheduled updates to these deliverables

.

Regulatory authorities reference the deliverables within their guidance documents

and the deliverables must be in alignment with the guidance documents. Stakeholders include regulatory authorities and organisations that create the regulatory referenced deliverables. The FDA expects sponsors to submit the deliverables

using the templates that PHUSE creates. Included in the PHUSE deliverables are the templates, example documents

and completion guidelines.