Prepare the case
Collect the minimum clinical information and identify missing imaging, pathology or history.
Selected organisations from Clinera's wider healthcare work
Clinera helps cancer centres make cases ready before the MDT, preserve the recommendation and coordinate the next action in one governed clinical workflow.
Designed for clinical teams, programme leaders, informatics and information governance.
Clinera connects case preparation, board coordination, decision capture and follow-up without turning the MDT into another administrative system.
Collect the minimum clinical information and identify missing imaging, pathology or history.
Bring the right specialties, cases and source materials into a shared meeting workflow.
Capture the recommendation, rationale and unresolved questions while the team is together.
Assign next steps, preserve the longitudinal record and report on completion.
Clinera has been shaped through MDT implementations, pilots, demonstrations and direct observation of tumour-board workflows across Egypt, Algeria, Nigeria and South Africa.
Standardised case preparation across tumour types and participating institutions.
Longitudinal decision history that remains available after the meeting ends.
Operational reporting for cases, attendance, recommendations and follow-up.
Structured and ad hoc collaboration for local, regional and expert-panel workflows.
Deployment starts with the centre's privacy, data-residency, integration and operating-model requirements—not a one-size-fits-all technology decision.
Clinera is designed to connect with institutional systems without creating an uncontrolled data pathway. Source-system access, mappings, data minimisation, governance and support are validated before implementation.
Documented API patterns support structured exchange with approved third-party and institutional systems.
Authentication, authorisation and role-aware access patterns protect the interfaces exposed to each deployment.
The data model uses FHIR resource concepts as an interoperability pathway for clinical information.
Versioning and API-documentation patterns support controlled integration and change management.
Standards boundary: references to FHIR, OAuth, REST or other standards describe documented architecture and design pathways. They do not imply product certification. Integration feasibility, conformance, security controls and ongoing support are confirmed for each deployment.
Each institution needs clear answers on who controls the data, where it is hosted, who can access it, what is logged, how long it is retained and what happens when the service ends.
Responsibilities are defined in the applicable service and data-processing agreements.
Institutions define the permitted purpose, users, roles and minimum information required for the workflow.
Managed cloud, private-cloud and on-premise patterns can be assessed against local requirements.
Logging, backups, retention, export and deletion obligations are set for the selected operating model.
Clinera supports the clinical, operational and governance teams responsible for making multidisciplinary cancer care work at scale.
Review complete cases and preserve the reasoning behind each recommendation.
Prepare boards, track missing information and coordinate what happens afterwards.
Standardise programmes and understand activity, adoption and operational performance.
Define hosting, access, integration, privacy and deployment responsibilities.
A nine-page brief for cancer-centre leaders, MDT programme owners, clinical informatics, IT and information governance.
Bring us the workflow, governance constraint or operational bottleneck you are trying to solve. We will assess fit with your clinical and implementation teams.