medicinal product authorizations

Create Medicinal Product Authorization

post
/organizations/{organizationId}/fhir/4/MedicinalProductAuthorization

The regulatory authorization of a medicinal product.

Request

Headers

content-type*stringapplication/json|application/json+fhirapplication/json
log-cdatastring
log-cdata-formatstringkv|jsonkv
AuthorizationstringBearer <token>

Params

organizationId*string|stringid|slug

Body

resourceType*This is a MedicinalProductAuthorization resource
ididThe logical id of the resource, as used in the URL for the resource. Once assigned, this value never changes.
metaMetaThe 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.
implicitRulesuriA 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.
languagecodeThe base language in which the resource is written.
textNarrativeA 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.
containedarray(ResourceList)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.
extensionarray(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.
modifierExtensionarray(Extension)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).
identifierarray(Identifier)Business identifier for the marketing authorization, as assigned by a regulator.
subjectReferenceThe medicinal product that is being authorized.
countryarray(CodeableConcept)The country in which the marketing authorization has been granted.
jurisdictionarray(CodeableConcept)Jurisdiction within a country.
statusCodeableConceptThe status of the marketing authorization.
statusDatedateTimeThe date at which the given status has become applicable.
restoreDatedateTimeThe date when a suspended the marketing or the marketing authorization of the product is anticipated to be restored.
validityPeriodPeriodThe 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.
dataExclusivityPeriodPeriodA period of time after authorization before generic product applicatiosn can be submitted.
dateOfFirstAuthorizationdateTimeThe date when the first authorization was granted by a Medicines Regulatory Agency.
internationalBirthDatedateTimeDate of first marketing authorization for a company's new medicinal product in any country in the World.
legalBasisCodeableConceptThe legal framework against which this authorization is granted.
jurisdictionalAuthorizationarray(MedicinalProductAuthorization_JurisdictionalAuthorization)Authorization in areas within a country.
holderReferenceMarketing Authorization Holder.
regulatorReferenceMedicines Regulatory Agency.
procedureMedicinalProductAuthorization_ProcedureThe regulatory procedure for granting or amending a marketing authorization.

Response

Patch Medicinal Product Authorization

patch
/organizations/{organizationId}/fhir/4/MedicinalProductAuthorization/{resourceId}

The regulatory authorization of a medicinal product.

Request

Headers

content-type*stringapplication/json-patch+jsonapplication/json-patch+json
log-cdatastring
log-cdata-formatstringkv|jsonkv
AuthorizationstringBearer <token>

Params

organizationId*string|stringid|slug
resourceId*

Body

resourceType*This is a MedicinalProductAuthorization resource
ididThe logical id of the resource, as used in the URL for the resource. Once assigned, this value never changes.
metaMetaThe 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.
implicitRulesuriA 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.
languagecodeThe base language in which the resource is written.
textNarrativeA 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.
containedarray(ResourceList)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.
extensionarray(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.
modifierExtensionarray(Extension)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).
identifierarray(Identifier)Business identifier for the marketing authorization, as assigned by a regulator.
subjectReferenceThe medicinal product that is being authorized.
countryarray(CodeableConcept)The country in which the marketing authorization has been granted.
jurisdictionarray(CodeableConcept)Jurisdiction within a country.
statusCodeableConceptThe status of the marketing authorization.
statusDatedateTimeThe date at which the given status has become applicable.
restoreDatedateTimeThe date when a suspended the marketing or the marketing authorization of the product is anticipated to be restored.
validityPeriodPeriodThe 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.
dataExclusivityPeriodPeriodA period of time after authorization before generic product applicatiosn can be submitted.
dateOfFirstAuthorizationdateTimeThe date when the first authorization was granted by a Medicines Regulatory Agency.
internationalBirthDatedateTimeDate of first marketing authorization for a company's new medicinal product in any country in the World.
legalBasisCodeableConceptThe legal framework against which this authorization is granted.
jurisdictionalAuthorizationarray(MedicinalProductAuthorization_JurisdictionalAuthorization)Authorization in areas within a country.
holderReferenceMarketing Authorization Holder.
regulatorReferenceMedicines Regulatory Agency.
procedureMedicinalProductAuthorization_ProcedureThe regulatory procedure for granting or amending a marketing authorization.

Response

Read Medicinal Product Authorization

get
/organizations/{organizationId}/fhir/4/MedicinalProductAuthorization/{resourceId}

Request

Headers

content-type*stringapplication/json|application/json+fhirapplication/json
log-cdatastring
log-cdata-formatstringkv|jsonkv
AuthorizationstringBearer <token>

Params

organizationId*string|stringid|slug
resourceId*

Response

Read History Medicinal Product Authorization

get
/organizations/{organizationId}/fhir/4/MedicinalProductAuthorization/{resourceId}/_history

Request

Headers

content-type*stringapplication/json|application/json+fhirapplication/json
log-cdatastring
log-cdata-formatstringkv|jsonkv
AuthorizationstringBearer <token>

Query params

_countstring
_sincestring

Params

organizationId*string|stringid|slug
resourceId*

Response

Read Version Medicinal Product Authorization

get
/organizations/{organizationId}/fhir/4/MedicinalProductAuthorization/{resourceId}/_history/{versionId}

Request

Headers

content-type*stringapplication/json|application/json+fhirapplication/json
log-cdatastring
log-cdata-formatstringkv|jsonkv
AuthorizationstringBearer <token>

Params

organizationId*string|stringid|slug
resourceId*
versionId*

Response

Remove Medicinal Product Authorization

delete
/organizations/{organizationId}/fhir/4/MedicinalProductAuthorization/{resourceId}

Request

Headers

content-type*stringapplication/json|application/json+fhirapplication/json
log-cdatastring
log-cdata-formatstringkv|jsonkv
AuthorizationstringBearer <token>

Params

organizationId*string|stringid|slug
resourceId*

Response

Search Get Medicinal Product Authorization

get
/organizations/{organizationId}/fhir/4/MedicinalProductAuthorization

Request

Headers

content-type*stringapplication/json|application/json+fhirapplication/json
log-cdatastring
log-cdata-formatstringkv|jsonkv
AuthorizationstringBearer <token>

Query params

_idstring
_languagestring
identifierstring
namestring
name-languagestring

Params

organizationId*string|stringid|slug

Response

Search History Medicinal Product Authorization

get
/organizations/{organizationId}/fhir/4/MedicinalProductAuthorization/_history

Request

Headers

content-type*stringapplication/json|application/json+fhirapplication/json
log-cdatastring
log-cdata-formatstringkv|jsonkv
AuthorizationstringBearer <token>

Query params

_countstring
_sincestring

Params

organizationId*string|stringid|slug

Response

Search Post Medicinal Product Authorization

post
/organizations/{organizationId}/fhir/4/MedicinalProductAuthorization/_search

The regulatory authorization of a medicinal product.

Request

Headers

content-type*stringapplication/json|application/x-www-form-urlencodedapplication/json
log-cdatastring
log-cdata-formatstringkv|jsonkv
AuthorizationstringBearer <token>

Query params

_idstring
_languagestring
identifierstring
namestring
name-languagestring

Params

organizationId*string|stringid|slug

Body

resourceType*This is a MedicinalProductAuthorization resource
ididThe logical id of the resource, as used in the URL for the resource. Once assigned, this value never changes.
metaMetaThe 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.
implicitRulesuriA 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.
languagecodeThe base language in which the resource is written.
textNarrativeA 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.
containedarray(ResourceList)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.
extensionarray(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.
modifierExtensionarray(Extension)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).
identifierarray(Identifier)Business identifier for the marketing authorization, as assigned by a regulator.
subjectReferenceThe medicinal product that is being authorized.
countryarray(CodeableConcept)The country in which the marketing authorization has been granted.
jurisdictionarray(CodeableConcept)Jurisdiction within a country.
statusCodeableConceptThe status of the marketing authorization.
statusDatedateTimeThe date at which the given status has become applicable.
restoreDatedateTimeThe date when a suspended the marketing or the marketing authorization of the product is anticipated to be restored.
validityPeriodPeriodThe 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.
dataExclusivityPeriodPeriodA period of time after authorization before generic product applicatiosn can be submitted.
dateOfFirstAuthorizationdateTimeThe date when the first authorization was granted by a Medicines Regulatory Agency.
internationalBirthDatedateTimeDate of first marketing authorization for a company's new medicinal product in any country in the World.
legalBasisCodeableConceptThe legal framework against which this authorization is granted.
jurisdictionalAuthorizationarray(MedicinalProductAuthorization_JurisdictionalAuthorization)Authorization in areas within a country.
holderReferenceMarketing Authorization Holder.
regulatorReferenceMedicines Regulatory Agency.
procedureMedicinalProductAuthorization_ProcedureThe regulatory procedure for granting or amending a marketing authorization.

Response

Update Medicinal Product Authorization

put
/organizations/{organizationId}/fhir/4/MedicinalProductAuthorization/{resourceId}

The regulatory authorization of a medicinal product.

Request

Headers

content-type*stringapplication/json|application/json+fhirapplication/json
log-cdatastring
log-cdata-formatstringkv|jsonkv
AuthorizationstringBearer <token>

Params

organizationId*string|stringid|slug
resourceId*

Body

resourceType*This is a MedicinalProductAuthorization resource
ididThe logical id of the resource, as used in the URL for the resource. Once assigned, this value never changes.
metaMetaThe 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.
implicitRulesuriA 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.
languagecodeThe base language in which the resource is written.
textNarrativeA 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.
containedarray(ResourceList)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.
extensionarray(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.
modifierExtensionarray(Extension)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).
identifierarray(Identifier)Business identifier for the marketing authorization, as assigned by a regulator.
subjectReferenceThe medicinal product that is being authorized.
countryarray(CodeableConcept)The country in which the marketing authorization has been granted.
jurisdictionarray(CodeableConcept)Jurisdiction within a country.
statusCodeableConceptThe status of the marketing authorization.
statusDatedateTimeThe date at which the given status has become applicable.
restoreDatedateTimeThe date when a suspended the marketing or the marketing authorization of the product is anticipated to be restored.
validityPeriodPeriodThe 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.
dataExclusivityPeriodPeriodA period of time after authorization before generic product applicatiosn can be submitted.
dateOfFirstAuthorizationdateTimeThe date when the first authorization was granted by a Medicines Regulatory Agency.
internationalBirthDatedateTimeDate of first marketing authorization for a company's new medicinal product in any country in the World.
legalBasisCodeableConceptThe legal framework against which this authorization is granted.
jurisdictionalAuthorizationarray(MedicinalProductAuthorization_JurisdictionalAuthorization)Authorization in areas within a country.
holderReferenceMarketing Authorization Holder.
regulatorReferenceMedicines Regulatory Agency.
procedureMedicinalProductAuthorization_ProcedureThe regulatory procedure for granting or amending a marketing authorization.

Response