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SPL documents are known as “product label,” “package insert,” “prescribing information,” “product information,” “medicines information,” and many other names. Global Membership Directory For members only. Promotes more coordinated data collection throughout the regulatory agency and improve processing, storage and archiving capabilities. This specification includes a detailed description of an information model for structured product labeling documents as well as the XML representation of that model.

CASE STUDIES See the Implementation Guide for this Standard. SPL documents can be exchanged across systems without the need for additional transformation steps.

Reduce or eliminate redundancies in data collection. Access the complete database of HL7 members with the option to search by name, organization, region or affiliate. The ability to provide the most up-to-date product labeling in a timely manner is considered to be critical to improving risk management of regulated products. Enhances patient safety by helping to provide prescribers and consumers with improved access to information needed to make better risk management decisions in a format that will enhance integration with other technical and clinical applications.

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Facilitates more efficient evaluation of labeling changes by allowing more effective use of computer technology to compare different versions of labeling on a section by section basis. Improves access to information and enhance the ability to query and report on the content of labeling, allowing better support for specific analyses such as sub-population assessments of differences in products based on gender, race, age, and geographic location. Global Membership Directory For members only. Enhances patient safety by helping to provide prescribers and consumers with improved access to information needed to make better risk management decisions in a format that will enhance integration with other technical and clinical applications.

Facilitates more efficient evaluation of labeling changes by allowing more effective use of computer technology to compare different versions of labeling on a section by section basis. SPL documents are known as “product label,” “package insert,” “prescribing information,” “product information,” “medicines information,” and many other names. Reduce or eliminate redundancies in data collection. The ability to provide the most up-to-date product labeling in a timely manner is considered to be critical to improving risk management of regulated products. Promotes more coordinated data collection throughout the regulatory agency and improve processing, storage and archiving capabilities. The ability to provide the most up-to-date product labeling in a timely manner is considered to be critical to improving risk management of regulated products.

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CASE STUDIES See the Implementation Guide for this Standard. Reduce or eliminate redundancies in data collection. This specification includes a detailed description of an information model for structured product labeling documents as well as the XML representation of that model. Global Membership Directory For members only.

Improves access to information and enhance the ability to query and report on the content of labeling, allowing better support for specific analyses such as sub-population assessments of differences in products based on gender, race, age, and geographic location. Promotes more coordinated data collection throughout the regulatory agency and improve processing, storage and archiving capabilities. SPL documents are known as “product label,” “package insert,” “prescribing information,” “product information,” “medicines information,” and many other names.

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Facilitates more efficient evaluation of labeling changes by allowing more effective use of computer technology to compare different versions of labeling on a section by section basis. Access the complete database of HL7 members with the option to search by name, organization, region or affiliate. Enhances patient safety by helping to provide prescribers and consumers with improved access to information needed to make better risk management decisions in a format that will enhance integration with other technical and clinical applications. Improves access to information and enhance the ability to query and report on the content of labeling, allowing better support for specific analyses such as sub-population assessments of differences in products based on gender, race, age, and geographic location. SPL documents can be exchanged across systems without the need for additional transformation steps.

Access the complete database of HL7 members with the option to search by name, organization, region or affiliate. This specification includes a detailed description of an information model for structured product labeling documents as well as the XML representation of that model. SPL documents can be exchanged across systems without the need for additional transformation steps. CASE STUDIES See the Implementation Guide for this Standard. This specification includes a detailed description of an information model for structured product labeling documents as well as the XML representation of that model. CASE STUDIES See the Implementation Guide for this Standard.

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Global Membership Directory For members only. SPL documents can be exchanged across systems without the need for additional transformation steps. Facilitates more efficient evaluation of labeling changes by allowing more effective use of computer technology to compare different versions of labeling on a section by section basis. The ability to provide the most up-to-date product labeling in a timely manner is considered to be critical to improving risk management of regulated products. Enhances patient safety by helping to provide prescribers and consumers with improved access to information needed to make better risk management decisions in a format that will enhance integration with other technical and clinical applications. This specification includes a detailed description of an information model for structured product labeling documents as well as the XML representation of that model.

SPL documents can be exchanged across systems without the need for additional transformation steps. Facilitates more efficient evaluation of labeling changes by allowing more effective use of computer technology to compare different versions of labeling on a section by section basis. CASE STUDIES See the Implementation Guide for this Standard.

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The ability to provide the most up-to-date product labeling in a timely manner is considered to be critical to improving risk management of regulated products. The ability to provide the most up-to-date product labeling in a timely manner is considered to be critical to improving risk management of regulated products. CASE STUDIES See the Implementation Guide for this Standard. Access the complete database of HL7 members with the option to search by name, organization, region or affiliate.

Enhances patient safety by helping to provide prescribers and consumers with improved access to information needed to make better risk management decisions in a format that will enhance integration with other technical and clinical applications. SPL documents are known as “product label,” “package insert,” “prescribing information,” “product information,” “medicines information,” and many other names. Reduce or eliminate redundancies in data collection. Promotes more coordinated data collection throughout the regulatory agency and improve processing, storage and archiving capabilities. Improves access to information and enhance the ability to query and report on the content of labeling, allowing better support for specific analyses such as sub-population assessments of differences in products based on gender, race, age, and geographic location.

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Access the complete database of HL7 members with the option to search by name, organization, region or affiliate. Improves access to information and enhance the ability to query and report on the content of labeling, allowing better support for specific analyses such as sub-population assessments of differences in products based on gender, race, age, and geographic location. Improves access to information and enhance the ability to query and report on the content of labeling, allowing better support for specific analyses such as sub-population assessments of differences in products based on gender, race, age, and geographic location.

Promotes more coordinated data collection throughout the regulatory agency and improve processing, storage and archiving capabilities. Reduce or eliminate redundancies in data collection. SPL documents are known as “product label,” “package insert,” “prescribing information,” “product information,” “medicines information,” and many other names. SPL documents can be exchanged across systems without the need for additional transformation steps.

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SPL documents are known as “product label,” “package insert,” “prescribing information,” “product information,” “medicines information,” and many other names. Access the complete database of HL7 members with the option to search by name, organization, region or affiliate. Promotes more coordinated data collection throughout the regulatory agency and improve processing, storage and archiving capabilities. Reduce or eliminate redundancies in data collection. Facilitates more efficient evaluation of labeling changes by allowing more effective use of computer technology to compare different versions of labeling on a section by section basis.

Global Membership Directory For members only. This specification includes a detailed description of an information model for structured product labeling documents as well as the XML representation of that model. Global Membership Directory For members only. Enhances patient safety by helping to provide prescribers and consumers with improved access to information needed to make better risk management decisions in a format that will enhance integration with other technical and clinical applications. Reduce or eliminate redundancies in data collection. This specification includes a detailed description of an information model for structured product labeling documents as well as the XML representation of that model.

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SPL documents can be exchanged across systems without the need for additional transformation steps. CASE STUDIES See the Implementation Guide for this Standard. Reduce or eliminate redundancies in data collection.

Access the complete database of HL7 members with the option to search by name, organization, region or affiliate. The ability to provide the most up-to-date product labeling in a timely manner is considered to be critical to improving risk management of regulated products. Enhances patient safety by helping to provide prescribers and consumers with improved access to information needed to make better risk management decisions in a format that will enhance integration with other technical and clinical applications.

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Improves access to information and enhance the ability to query and report on the content of labeling, allowing better support for specific analyses such as sub-population assessments of differences in products based on gender, race, age, and geographic location. Facilitates more efficient evaluation of labeling changes by allowing more effective use of computer technology to compare different versions of labeling on a section by section basis. SPL documents can be exchanged across systems without the need for additional transformation steps. This specification includes a detailed description of an information model for structured product labeling documents as well as the XML representation of that model.

Improves access to information and enhance the ability to query and report on the content of labeling, allowing better support for specific analyses such as sub-population assessments of differences in products based on gender, race, age, and geographic location. Promotes more coordinated data collection throughout the regulatory agency and improve processing, storage and archiving capabilities. The ability to provide the most up-to-date product labeling in a timely manner is considered to be critical to improving risk management of regulated products.