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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. Drug listing data elements include coded information about the product (including product and generic names, ingredients, ingredient strengths, dosage forms, routes of administration, appearance, dea schedule) and the packaging (package quantity and type).

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    Improves interoperability of the regulatory agencys systems with other clinical information systems 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 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. Implementation guide provides technical conformance criteria for spl  files based on the drug establishment registration and drug listing process at the united states food and drug administration (fda).

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