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Category
Supplementary Resource
Type
Standard
Version
1.1
Access
Open
Status
Active
Created
September 2017
This white paper describes the requirements and constraints for patient demographic data that should be collected and exchanged for patient registration. These data requirements may be proposed to be published as a future IHE Technical Framework Volume 4 US National Extension to the IHE ITI Patient Administration Management (PAM) Profile for the message-based data exchange.

Main sections:

- Introduction

- Patient registration

- Overview of proposed national extension to the technical framework

- Proposed national extension for IHE United States
Access IHE Patient Care Coordination (PCC) White Paper - Patient Registration Demographics Data Capture and Exchange v1.1

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