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HL7 Version 3 Standard: Structured Product Labeling, Release 4

Structured Product Labeling, Release 2. HL7 Version 3 Implementation Guide: Clinical data elements include coded information about the clinical use of the product including indications and use, contraindications, drug interactions, warning and precautions and use in special populations. Structured Product Labeling, Release 1. Structured Product Labeling, Release 4 may also go by the following names or acronyms:. Structured Product Labeling, Release 3.
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HL7 Standards Product Brief - HL7 Version 3 Standard: Structured Product Labeling, Release 4

For specifications and information about workgroups, training, projects and more, visit the HL7 Wiki page for this product at:. SPL documents contain both the content of labeling all text, tables and figures for a product along with additional machine readable information including drug listing data elements and clinical data elements. Structured Product Labeling, Release 4 may also go by the following names or acronyms: Clinical data elements include coded information about the clinical use of the product including indications and use, contraindications, drug interactions, warning and precautions and use in special populations.
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Description: SPL documents contain both the content of labeling all text, tables and figures for a product along with additional machine readable information including drug listing data elements and clinical data elements. Global Membership Directory For members only. HL7 Version 3 Implementation Guide: The HL7 Version 3 Structured Product Labeling SPL specification is a document markup standard that specifies the structure and semantics of the content of authorized published information that accompanies any medicine licensed by a medicines licensing authority. An SPL document is created by an organization that is required by law to submit product information document because it is responsible for the creation or marketing of a product, or any other person or organization compelled by other motives to submit information about products, whether originally created or not.

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