spark_auto_mapper_fhir.resources.medicinal_product_authorization

Module Contents

Classes

MedicinalProductAuthorization

MedicinalProductAuthorization
class spark_auto_mapper_fhir.resources.medicinal_product_authorization.MedicinalProductAuthorization(*, id_=None, meta=None, implicitRules=None, language=None, text=None, contained=None, extension=None, modifierExtension=None, identifier=None, subject=None, country=None, jurisdiction=None, status=None, statusDate=None, restoreDate=None, validityPeriod=None, dataExclusivityPeriod=None, dateOfFirstAuthorization=None, internationalBirthDate=None, legalBasis=None, jurisdictionalAuthorization=None, holder=None, regulator=None, procedure=None)

Bases: spark_auto_mapper_fhir.base_types.fhir_resource_base.FhirResourceBase

MedicinalProductAuthorization medicinalproductauthorization.xsd

The regulatory authorization of a medicinal product. If the element is present, it must have either a @value, an @id, or extensions

The regulatory authorization of a medicinal product. If the element is present, it must have either a @value, an @id, or extensions

param id_

The logical id of the resource, as used in the URL for the resource. Once

assigned, this value never changes.
param meta

The metadata about the resource. This is content that is maintained by the

infrastructure. Changes to the content might not always be associated with version changes to the resource.

param implicitRules

A reference to a set of rules that were followed when the resource was

constructed, and which must be understood when processing the content. Often, this is a reference to an implementation guide that defines the special rules along with other profiles etc.

param language

The base language in which the resource is written.

param text

A human-readable narrative that contains a summary of the resource and can be

used to represent the content of the resource to a human. The narrative need not encode all the structured data, but is required to contain sufficient detail to make it “clinically safe” for a human to just read the narrative. Resource definitions may define what content should be represented in the narrative to ensure clinical safety.

param contained

These resources do not have an independent existence apart from the resource

that contains them - they cannot be identified independently, and nor can they have their own independent transaction scope.

param extension

May be used to represent additional information that is not part of the basic

definition of the resource. To make the use of extensions safe and manageable, there is a strict set of governance applied to the definition and use of extensions. Though any implementer can define an extension, there is a set of requirements that SHALL be met as part of the definition of the extension.

param modifierExtension

May be used to represent additional information that is not part of the basic

definition of the resource and that modifies the understanding of the element that contains it and/or the understanding of the containing element’s descendants. Usually modifier elements provide negation or qualification. To make the use of extensions safe and manageable, there is a strict set of governance applied to the definition and use of extensions. Though any implementer is allowed to define an extension, there is a set of requirements that SHALL be met as part of the definition of the extension. Applications processing a resource are required to check for modifier extensions.

Modifier extensions SHALL NOT change the meaning of any elements on Resource or DomainResource (including cannot change the meaning of modifierExtension itself).

param identifier

Business identifier for the marketing authorization, as assigned by a

regulator.
param subject

The medicinal product that is being authorized.

param country

The country in which the marketing authorization has been granted.

param jurisdiction

Jurisdiction within a country.

param status

The status of the marketing authorization.

param statusDate

The date at which the given status has become applicable.

param restoreDate

The date when a suspended the marketing or the marketing authorization of the

product is anticipated to be restored.
param validityPeriod

The beginning of the time period in which the marketing authorization is in

the specific status shall be specified A complete date consisting of day, month and year shall be specified using the ISO 8601 date format.

param dataExclusivityPeriod

A period of time after authorization before generic product applicatiosn can

be submitted.
param dateOfFirstAuthorization

The date when the first authorization was granted by a Medicines Regulatory

Agency.
param internationalBirthDate

Date of first marketing authorization for a company’s new medicinal product in

any country in the World.
param legalBasis

The legal framework against which this authorization is granted.

param jurisdictionalAuthorization

Authorization in areas within a country.

param holder

Marketing Authorization Holder.

param regulator

Medicines Regulatory Agency.

param procedure

The regulatory procedure for granting or amending a marketing authorization.

Parameters
get_schema(self, include_extension)
Parameters

include_extension (bool) –

Return type

Optional[Union[pyspark.sql.types.StructType, pyspark.sql.types.DataType]]