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<p><span lang="EN-GB">This document provides requirements and recommendations related to the concepts required to associate pharmaceutical products or groups of pharmaceutical products with an appropriate set of PhPID(s) in accordance with </span><span lang="EN-GB">ISO 11616</span><span lang="EN-GB">.</span></p>
<p><span lang="EN-GB">Pharmaceutical product identifiers and the related elements are intended to represent pharmaceutical products as defined within a medicinal product by a medicines regulatory authority. While the ISO standards on IDMP can be applied to off-label usage of medicinal products, such applications are currently outside of the scope of this document.</span></p>
<p><span lang="EN-GB">Reference to </span><span lang="EN-GB">ISO 11238</span><span lang="EN-GB">, </span><span lang="EN-GB">ISO 11239</span><span lang="EN-GB">, </span><span lang="EN-GB">ISO 11240</span><span lang="EN-GB">, </span><span lang="EN-GB">ISO 11615</span><span lang="EN-GB">, HL7 V3 messaging standards (HL7 Reference Information Model (RIM)</span>[8]<span lang="EN-GB">, HL7 Common Product Model (CPM)</span><sup>[9]</sup><span lang="EN-GB"> and HL7 V3 Structured Product Labelling (SPL)</span><sup>[10]</sup><span lang="EN-GB">, and HL7 FHIR</span><sup>[11]</sup><span lang="EN-GB"> can be applied for pharmaceutical product information in the context of this document.</span></p>
Reģistrācijas numurs (WIID)
86407
Darbības sfēra
<p><span lang="EN-GB">This document provides requirements and recommendations related to the concepts required to associate pharmaceutical products or groups of pharmaceutical products with an appropriate set of PhPID(s) in accordance with </span><span lang="EN-GB">ISO 11616</span><span lang="EN-GB">.</span></p>
<p><span lang="EN-GB">Pharmaceutical product identifiers and the related elements are intended to represent pharmaceutical products as defined within a medicinal product by a medicines regulatory authority. While the ISO standards on IDMP can be applied to off-label usage of medicinal products, such applications are currently outside of the scope of this document.</span></p>
<p><span lang="EN-GB">Reference to </span><span lang="EN-GB">ISO 11238</span><span lang="EN-GB">, </span><span lang="EN-GB">ISO 11239</span><span lang="EN-GB">, </span><span lang="EN-GB">ISO 11240</span><span lang="EN-GB">, </span><span lang="EN-GB">ISO 11615</span><span lang="EN-GB">, HL7 V3 messaging standards (HL7 Reference Information Model (RIM)</span>[8]<span lang="EN-GB">, HL7 Common Product Model (CPM)</span><sup>[9]</sup><span lang="EN-GB"> and HL7 V3 Structured Product Labelling (SPL)</span><sup>[10]</sup><span lang="EN-GB">, and HL7 FHIR</span><sup>[11]</sup><span lang="EN-GB"> can be applied for pharmaceutical product information in the context of this document.</span></p>
