This page is part of the Pharmaceutical Quality (Industry) (v1.0.0-ballot: STU1 Ballot 1) based on FHIR (HL7® FHIR® Standard) v5.0.0. . For a full list of available versions, see the Directory of published versions
Downloads
Full Implementation Guide
The entire implementation guide (including the HTML files, definitions, validation information, etc.) may be downloaded here.
In addition there are format specific definitions files.
Examples: all the examples that are used in this Implementation Guide available for download:
Cross Version Analysis
Dependency Table
Package hl7.fhir.uv.extensions.r5#1.0.0
This IG defines the global extensions - the ones defined for everyone. These extensions are always in scope wherever FHIR is being used (built Sun, Mar 26, 2023 08:46+1100+11:00)
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Global Profiles Table
There are no Global profiles defined
IP Statements
This publication includes IP covered under the following statements.
- ISO Maintains the copyright on the country codes, and controls it's use carefully. For futher details see the ISO 3166 web page: https://www.iso.org/iso-3166-country-codes.html
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- The UCUM codes, UCUM table (regardless of format), and UCUM Specification are copyright 1999-2009, Regenstrief Institute, Inc. and the Unified Codes for Units of Measures (UCUM) Organization. All rights reserved. https://ucum.org/trac/wiki/TermsOfUse
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- Unified Code for Units of Measure (UCUM): Bundle/bundle-batch-analysis-pq-ex1-prod, Bundle/bundle-batch-analysis-pq-ex2-sub... Show 22 more, Bundle/bundle-drug-reference-standards-pq-ex2-sub, Bundle/bundle-drug-stability-pq-ex1-prod, Bundle/bundle-drug-stability-pq-ex2-sub, Bundle/bundle-drug-substance-characterization-pq-ex1, Bundle/bundle-drug-substance-specification-pq-ex1, Bundle/bundle-product-impurities-pq-ex1, Bundle/bundle-product-impurities-pq-ex2-sub, Bundle/bundle-product-manufacturing-pq-ex1, Bundle/bundle-product-manufacturing-pq-ex2-sub, Bundle/bundle-product-process-validation-pq-ex1, Bundle/bundle-product-process-validation-pq-ex2-sub, Bundle/bundle-product-process-validation-pq-ex3-prod-bio, MedicinalProductDefinitionDrugProductPq, Observation/observation-test-result-lt25c-i1-degradation-imp-total, Observation/observation-test-result-lt25c-i1-degradation-imp-unspecified, Observation/observation-test-result-lt25c-i1-degradation-imp1, Observation/observation-test-result-lt25c-i1-degradation-imp2, Observation/observation-test-result-lt25c-i1-degradation-imp3, Observation/observation-test-result-lt25c-i1-water, ObservationDefinition/Degradation, ObservationDefinition/Water and PlanDefinition/plandefinition-drug-pq-ex5-stability-study-protocol
- This material contains content that is copyright of SNOMED International. Implementers of these specifications must have the appropriate SNOMED CT Affiliate license - for more information contact https://www.snomed.org/get-snomed or info@snomed.org.
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