ISO-27953-2 › Health informatics - Individual case safety reports (ICSRs) in pharmacovigilance - Part 2: Human pharmaceutical reporting requirements for ICSR

ISO-27953-2 - 1ST EDITION REPRINT - CURRENT
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ISO 27593-2:2011 seeks to create a standardized framework for international regulatory reporting and information sharing by providing a common set of data elements and a messaging format for transmission of ICSRs for adverse drug reactions (ADR), adverse events (AE), infections, and incidents that can occur upon the administration of one or more human pharmaceutical products to a patient, regardless of source and destination.

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Document Number

ISO/HL7 27953-2:2011

Revision Level

1ST EDITION REPRINT

Status

Current

Publication Date

Oct. 15, 2012

Committee Number

ISO/TC 215