This page is part of the FHIR Specification (v5.0.0: R5 - STU). This is the current published version. For a full list of available versions, see the Directory of published versions . Page versions: R5 R4B
Biomedical Research and Regulation Work Group | Maturity Level: N/A | Standards Status: Informative | Compartments: No defined compartments |
ShEx statement for regulatedauthorization
PREFIX fhir: <http://hl7.org/fhir/> PREFIX fhirvs: <http://hl7.org/fhir/ValueSet/> PREFIX xsd: <http://www.w3.org/2001/XMLSchema#> PREFIX rdf: <http://www.w3.org/1999/02/22-rdf-syntax-ns#> IMPORT <Period.shex> IMPORT <markdown.shex> IMPORT <dateTime.shex> IMPORT <Location.shex> IMPORT <Reference.shex> IMPORT <Identifier.shex> IMPORT <Ingredient.shex> IMPORT <Organization.shex> IMPORT <Practitioner.shex> IMPORT <ResearchStudy.shex> IMPORT <DomainResource.shex> IMPORT <PlanDefinition.shex> IMPORT <CodeableConcept.shex> IMPORT <BackboneElement.shex> IMPORT <DeviceDefinition.shex> IMPORT <NutritionProduct.shex> IMPORT <CodeableReference.shex> IMPORT <DocumentReference.shex> IMPORT <ActivityDefinition.shex> IMPORT <SubstanceDefinition.shex> IMPORT <ObservationDefinition.shex> IMPORT <PackagedProductDefinition.shex> IMPORT <BiologicallyDerivedProduct.shex> IMPORT <ManufacturedItemDefinition.shex> IMPORT <MedicinalProductDefinition.shex> start=@<RegulatedAuthorization> AND {fhir:nodeRole [fhir:treeRoot]} # Regulatory approval, clearance or licencing related to a regulated product, treatment, facility or activity e.g. Market Authorization for a Medicinal Product <RegulatedAuthorization> EXTENDS @<DomainResource> CLOSED { a [fhir:RegulatedAuthorization]?; fhir:nodeRole [fhir:treeRoot]?; fhir:identifier @<OneOrMore_Identifier>?; # Business identifier for the # authorization, typically assigned # by the authorizing body fhir:subject @<OneOrMore_Reference_ActivityDefinition_OR_BiologicallyDerivedProduct_OR_DeviceDefinition_OR_Ingredient_OR_Location_OR_ManufacturedItemDefinition_OR_MedicinalProductDefinition_OR_NutritionProduct_OR_ObservationDefinition_OR_Organization_OR_PackagedProductDefinition_OR_PlanDefinition_OR_Practitioner_OR_ResearchStudy_OR_SubstanceDefinition>?; # The product type, treatment, # facility or activity that is being # authorized fhir:type @<CodeableConcept>?; # Overall type of this # authorization, for example drug # marketing approval, orphan drug # designation fhir:description @<markdown>?; # General textual supporting # information fhir:region @<OneOrMore_CodeableConcept>?; # The territory in which the # authorization has been granted fhir:status @<CodeableConcept>?; # The status that is authorised e.g. # approved. Intermediate states can # be tracked with cases and # applications fhir:statusDate @<dateTime>?; # The date at which the current # status was assigned fhir:validityPeriod @<Period>?; # The time period in which the # regulatory approval etc. is in # effect, e.g. a Marketing # Authorization includes the date of # authorization and/or expiration # date fhir:indication @<OneOrMore_CodeableReference>?; # Condition for which the use of the # regulated product applies fhir:intendedUse @<CodeableConcept>?; # The intended use of the product, # e.g. prevention, treatment fhir:basis @<OneOrMore_CodeableConcept>?; # The legal/regulatory framework or # reasons under which this # authorization is granted fhir:holder @<Reference> AND {fhir:link @<Organization> ? }?; # The organization that has been # granted this authorization, by the # regulator fhir:regulator @<Reference> AND {fhir:link @<Organization> ? }?; # The regulatory authority or # authorizing body granting the # authorization fhir:attachedDocument @<OneOrMore_Reference_DocumentReference>?; # Additional information or # supporting documentation about the # authorization fhir:case @<RegulatedAuthorization.case>?; # The case or regulatory procedure # for granting or amending a # regulated authorization. Note: # This area is subject to ongoing # review and the workgroup is # seeking implementer feedback on # its use (see link at bottom of # page) } # The case or regulatory procedure for granting or amending a regulated authorization. Note: This area is subject to ongoing review and the workgroup is seeking implementer feedback on its use (see link at bottom of page) <RegulatedAuthorization.case> EXTENDS @<BackboneElement> CLOSED { fhir:identifier @<Identifier>?; # Identifier by which this case can # be referenced fhir:type @<CodeableConcept>?; # The defining type of case fhir:status @<CodeableConcept>?; # The status associated with the case fhir:date @<Period> OR @<dateTime> ?; # Relevant date for this case fhir:application @<OneOrMore_RegulatedAuthorization.case>?; # Applications submitted to obtain a # regulated authorization. Steps # within the longer running case or # procedure } # Applications submitted to obtain a regulated authorization. Steps within the longer running case or procedure <RegulatedAuthorization.case.applicationnull> CLOSED { } #---------------------- Cardinality Types (OneOrMore) ------------------- <OneOrMore_Identifier> CLOSED { rdf:first @<Identifier> ; rdf:rest [rdf:nil] OR @<OneOrMore_Identifier> } <OneOrMore_Reference_ActivityDefinition_OR_BiologicallyDerivedProduct_OR_DeviceDefinition_OR_Ingredient_OR_Location_OR_ManufacturedItemDefinition_OR_MedicinalProductDefinition_OR_NutritionProduct_OR_ObservationDefinition_OR_Organization_OR_PackagedProductDefinition_OR_PlanDefinition_OR_Practitioner_OR_ResearchStudy_OR_SubstanceDefinition> CLOSED { rdf:first @<Reference> AND {fhir:link @<ActivityDefinition> OR @<BiologicallyDerivedProduct> OR @<DeviceDefinition> OR @<Ingredient> OR @<Location> OR @<ManufacturedItemDefinition> OR @<MedicinalProductDefinition> OR @<NutritionProduct> OR @<ObservationDefinition> OR @<Organization> OR @<PackagedProductDefinition> OR @<PlanDefinition> OR @<Practitioner> OR @<ResearchStudy> OR @<SubstanceDefinition> } ; rdf:rest [rdf:nil] OR @<OneOrMore_Reference_ActivityDefinition_OR_BiologicallyDerivedProduct_OR_DeviceDefinition_OR_Ingredient_OR_Location_OR_ManufacturedItemDefinition_OR_MedicinalProductDefinition_OR_NutritionProduct_OR_ObservationDefinition_OR_Organization_OR_PackagedProductDefinition_OR_PlanDefinition_OR_Practitioner_OR_ResearchStudy_OR_SubstanceDefinition> } <OneOrMore_CodeableConcept> CLOSED { rdf:first @<CodeableConcept> ; rdf:rest [rdf:nil] OR @<OneOrMore_CodeableConcept> } <OneOrMore_CodeableReference> CLOSED { rdf:first @<CodeableReference> ; rdf:rest [rdf:nil] OR @<OneOrMore_CodeableReference> } <OneOrMore_Reference_DocumentReference> CLOSED { rdf:first @<Reference> AND {fhir:link @<DocumentReference> } ; rdf:rest [rdf:nil] OR @<OneOrMore_Reference_DocumentReference> } <OneOrMore_RegulatedAuthorization.case> CLOSED { rdf:first @<RegulatedAuthorization.case> ; rdf:rest [rdf:nil] OR @<OneOrMore_RegulatedAuthorization.case> }
Usage note: every effort has been made to ensure that the ShEx files are correct and useful, but they are not a normative part of the specification.
FHIR ®© HL7.org 2011+. FHIR R5 hl7.fhir.core#5.0.0 generated on Sun, Mar 26, 2023 15:25+1100.
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