This scenario documents a vitamin D3 supplement as a fully described medicinal product for regulatory and supply-chain contexts. It includes marketing authorization, ingredient composition, manufactured and packaged presentations, and pharmaceutical properties appropriate to an over-the-counter nutritional product with established labeling. Contraindications, indications, interactions, and undesirable effects are represented in line with standard product information, all in proportionate, non-alarming language suitable for reference data and catalog feeds.
from zato_fhir.test.r4.v1 import Scenarios, TestData
for instance in Scenarios.product_registration:
mp = instance.medicinal_product
print(mp.type_)
auth = instance.medicinal_product_authorization
print(auth.status)
ing = instance.medicinal_product_ingredient
print(ing.role)
mfg = instance.medicinal_product_manufactured
print(mfg.manufacturedDoseForm)
pkg = instance.medicinal_product_packaged
print(pkg.legalStatusOfSupply)
pharm = instance.medicinal_product_pharmaceutical
print(pharm.administrableDoseForm)
ci = instance.medicinal_product_contraindication
print(ci.id)
ind = instance.medicinal_product_indication
print(ind.id)
inter = instance.medicinal_product_interaction
print(inter.id)
ue = instance.medicinal_product_undesirable
print(ue.id)This scenario documents a vitamin D3 supplement as a fully described medicinal product for regulatory and supply-chain contexts. It includes marketing authorization, ingredient composition, manufactured and packaged presentations, and pharmaceutical properties appropriate to an over-the-counter nutritional product with established labeling. Contraindications, indications, interactions, and undesirable effects are represented in line with standard product information, all in proportionate, non-alarming language suitable for reference data and catalog feeds.
No patient appears in this scenario because the focus is entirely on the product and its regulatory artifacts. The bundle supports testing of pharmaceutical catalogs, formulary interfaces, and conformance to medicinal product-related profiles without mixing clinical encounters into the same instance.
10 resources per instance, 100 total across 10 instances.
| FHIR resource type | Role in this scenario |
|---|---|
MedicinalProduct | Core product identity for the vitamin D3 supplement |
MedicinalProductAuthorization | Regulatory authorization or registration details |
MedicinalProductIngredient | Active and excipient ingredients |
MedicinalProductManufactured | Manufactured presentation of the product |
MedicinalProductPackaged | Packaged trade item details |
MedicinalProductPharmaceutical | Pharmaceutical characteristics of the dose form |
MedicinalProductContraindication | Documented contraindications |
MedicinalProductIndication | Approved or labeled indications |
MedicinalProductInteraction | Known interaction considerations |
MedicinalProductUndesirableEffect | Undesirable effects for product labeling |
FHIR resources per instance | 10 |
Total resources (10 instances) | 100 |
Distinct resource types | 10 |
Scenario identifier | `Scenarios.product_registration` |
Get started with Zato and connect your systems in minutes.