Universal API Implementation Guide
1.1.20 - ci-build
Universal API Implementation Guide - Local Development build (v1.1.20) built by the FHIR (HL7® FHIR® Standard) Build Tools. See the Directory of published versions
IMPORTANT:
Access to Ocrevus Copay Questionnaire
Questionnaires for Ocrevus Copay enrollments can be accessed by requesting questionnaire definitions from the Genentech FHIR Server.
URL to Copay Questionnaire endpoint (test): https://test-us-e1.apis.roche.com/pharma-cmg-copay-exp-test/v1/questionnaire?name=Copay Ocrevus
URL to Copay Questionnaire endpoint (stage): https://stage-us-e1.apis.roche.com/pharma-cmg-copay-exp-stage/v1/questionnaire?name=Copay Ocrevus
URLto Copay Questionnaire endpoint (prod): https://prod-us-e1.apis.roche.com/pharma-cmg-copay-exp-prod/v1/questionnaire?name=Copay Ocrevus
Type | Available in QA (test) environment? | Product(s) impacted | linkId impacted (if applicable) | OLD | New | Comments | |
---|---|---|---|---|---|---|---|
Addition | Yes | Ocrevus | ocrevus-form-of-ocrevus | - | "linkId": "ocrevus-form-of-ocrevus", "text": "Which form of OCREVUS is the patient taking?", "type": "choice", "required": true, "repeats": false, "answerOption": [ { "valueString": "Intravenous infusion (IV) for OCREVUS" }, { "valueString": "Subcutaneous (SC) injection for OCREVUS ZUNOVO" } |
IMPORTANT: Genentech will deploy to production on evening of 2024-OCT-4. CRX will deploy a validation for this questionnaire on 2024-OCT-8. If this question is missing from the Copay request bundle, CRX will generate an error and enrollment will not be processed. |
|
Update | Yes | Ocrevus | ocrevus-fda-approved-indications | "linkId": "ocrevus-fda-approved-indications", "text": "Is the patient using OCREVUS for the following FDA-approved indication?", |
"linkId": "ocrevus-fda-approved-indications", "text": "Is the patient using OCREVUS or OCREVUS ZUNOVO for the following FDA-approved indication?", |
Change in text |
Ocrevus Zunovo Copay questionnaires are the same as the Ocrevus Copay questionnaires but with a few additions/updates.
Type | Available in QA (test) environment? | Product(s) impacted | linkId impacted (if applicable) | OLD | New | Comments | |
---|---|---|---|---|---|---|---|
Addition | Yes | Ocrevus Zunovo | ocrevus-zunovo-form-of-ocrevus | - | "linkId": "ocrevus-zunovo-form-of-ocrevus", "text": "Which form of OCREVUS is the patient taking?", "type": "choice", "required": true, "repeats": false, "answerOption": [ { "valueString": "Intravenous infusion (IV) for OCREVUS" }, { "valueString": "Subcutaneous (SC) injection for OCREVUS ZUNOVO" } |
IMPORTANT: Genentech will deploy to production on evening of 2024-OCT-4. CRX will deploy a validation for this questionnaire on 2024-OCT-8. If this question is missing from the Copay request bundle, CRX will generate an error and enrollment will not be processed. |
|
Addition | Yes | Ocrevus Zunovo | ocrevus-zunovo-fda-approved-indications | - | Same Copay questionnaire configuration as Ocrevus Copay indication: "linkId": "ocrevus-zunovo-fda-approved-indications", "text": "Is the patient using OCREVUS or OCREVUS ZUNOVO for the following FDA-approved indication?", "type": "choice", "required": true, "repeats": false, "answerOption": [ { "valueCoding": { "code": "Relapsing-forms-of-multiple-sclerosis-(MS)-to-include-clinically-isolated-syndrome-relapsing-remitting-disease-and-active-secondary-progressive-disease-or-primary-progressive-forms-of-MS-in-adults", "display": "Relapsing forms of multiple sclerosis (MS), to include clinically isolated syndrome, relapsing-remitting disease and active secondary progressive disease or primary progressive forms of MS, in adults" } }, { "valueCoding": { "code": "no", "display": "No" } }, { "valueCoding": { "code": "unsure", "display": "Unsure" } } |
Refer to brandIds table on Copay Value Set page
FDA approved indications (ICD10 codes) can be found on the Access Solutions website for Ocrevus Zunovo