Here you can find all of the information needed to register a patient in the BSRBR-RA.
Clinical baseline documents are required for each new patient registered in the BSRBR-RA.
Please ensure you consult the eligibility checker (PDF, 99KB) to confirm that the patient is eligible for the BSRBR-RA before recruiting them.
Once you have completed all of the registration documents (as listed on our Enrolling a Participant Checklist) please post them to the BSRBR-RA offices.
We will then register the patient and inform you of when their next follow-up is due.
We will also send out a patient baseline form directly to the patient with their first six monthly diary.
Forms for registering patients new to the BSRBR-RA on biologic or biosimilar therapy
- Consultant Baseline Form (PDF, 189KB)
- Patient Information Sheet (Word .docx, 801KB)
- Patient Consent Form (Word .docx, 751KB)
- Health Assessment Questionnaire (HAQ) (PDF, 15KB)
- Patient Baseline EuroQol (EQ-5D) (PDF, 559KB)
Forms for re-registering/switching patients on biologic or biosimilar therapy who are already participating in the BSRBR-RA
If your patient is already on the Register, they may be eligible to be re-registered with the BSRBR-RA. Full details on this, and all other aspects of re-registering patients can be found in the BSRBR-RA Re-registration Guide.
To re-register patients, we need their current BSRBR-RA ID, HAQ and EQ-5D plus a copy of the signed consent form.
Please click on the links below to access re-registration forms for patients who have been registered to the BSRBR-RA before: