Cross-site patient records
Cross-site record access is not launch-authorised until the group approves purpose, lawful basis, role mapping, recipient/site boundaries, DPIA and access tests.
Multi-site operations
Built for groups, not just for clinics.
Group-wide reporting
Staff-reviewed operational and revenue views by authorised scope. Clinical-outcome reporting and scheduled exports require clinic acceptance evidence.
SSO, SAML & SCIM — disabled
No enterprise identity/provisioning route is launch-authorised. Provider terms, least privilege, offboarding and production authentication evidence are required.
Role-based access
Role controls are implemented, but each site must validate least privilege, privileged access, offboarding and defined-event logging before launch.
Unified billing
Stripe and invoice ownership are configured per signed commercial/clinic structure. Automated PCRS submission is not launch-authorised.
Brigid for groups
Approved templates and staff-controlled scheduling by authorised site. Cross-site rebooking and group care campaigns require separate approval.
Enterprise onboarding
Phased evidence, site-by-site approval.
- Phase 1
Scope & accountability
The group identifies controllers, sites, purposes, roles, systems and prohibited cross-site flows. Delivery responsibilities are recorded in the signed plan.
- Phase 2
Phased site migration
Migrate in an agreed sequence with representative imports, role tests, continuity and rollback. No site cuts over until it accepts the evidence; no zero-loss or zero-downtime promise is made without a tested plan.
- Phase 3
Group-wide reporting + go-live
Validate group reporting and authorised cross-site workflows. Support cadence is stated in the signed order form rather than assumed here.
Questions group operators ask
Things that come up on every architecture call.
- Can we keep our existing IT?
- No compatibility or replacement claim is made without an interface inventory and validated integration plan. SSO/SCIM and named imaging/lab connections are disabled unless their provider, security and production evidence is approved.
- What does data isolation look like across sites?
- Tenant and role boundaries are validated per site. Cross-site health-record sharing is disabled for launch unless the controller approves the purpose, lawful basis, Article 9 condition, DPIA, access, revocation and logging tests.
- Do you support SCIM provisioning?
- SCIM 2.0 automated provisioning for Microsoft Entra ID, Okta and Google Workspace is on our enterprise roadmap. Today, clinicians and admins are provisioned through Brigid’s own role management. Talk to us about timelines for your rollout.
- How do we report across sites?
- Approved operational and revenue fields can be reported within authorised group scope. Clinical-outcome reporting and scheduled exports require separate validation and recipient controls.
- What if a site needs to leave the group?
- Exit scope, format, encryption, assistance, timing, deletion and any fees are stated in the signed agreement and tested exit plan. The group verifies a representative export before go-live.
Built for groups
Site-by-site approval before cross-site operation.
- Disabled
- Cross-site health-record sharing
- Required
- Controller and role mapping
- Per site
- Acceptance and rollback evidence
- Signed
- Support and delivery ownership
Talk it through with us.
Discuss the proposed scope. Any delivery, support, integration or timeline commitment must be recorded in the signed order and implementation plan.
Talk to salesBlog
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