Healthcare Record Source Layers
This page is the canonical routing map for source-layer labels used in healthcare-recording synthesis tables. Use it when a visible wiki table says "GMC", "NMC", "provider governance", "NHS information standards", "records-management code", or similar shorthand.
The Source Register remains the source of truth for provenance. This page prevents source-layer labels from becoming unexplained acronyms or unsupported prose.
Source-Layer Map
| Source-layer label | Use for | Canonical page | Boundary |
|---|---|---|---|
| GMC medical professional duties | Doctor record keeping, consent, confidentiality, candour, patient communication, decisions, and review responsibility. | GMC Record Keeping and Professional Duties | Professional duty evidence, not provider governance or product compliance. |
| NMC professional duties | Nursing, midwifery, and nursing-associate record keeping, risk/action recording, attribution, date/time, and security. | NMC Record Keeping and Professional Duties | Professional duty evidence, not a full care-record content model. |
| HCPC professional duties | Allied-health and HCPC registrant record keeping across professional settings. | HCPC Record Keeping and Professional Duties | Profession-specific content still depends on role, setting, and local policy. |
| GPhC pharmacy duties | Pharmacy consent, prescribing, confidentiality, record use, and person-centred pharmacy service evidence. | GPhC Record Keeping and Pharmacy Duties | Pharmacy professional evidence, not GP foundation or GP Connect assurance. |
| Provider governance | Registered-provider governance records, secure/accurate/complete/contemporaneous care records, and England CQC duties. | CQC Provider Governance | England CQC evidence; devolved provider duties need nation-specific sources. |
| Candour | Incident disclosure, apology, written follow-up, correspondence, organisational candour, and professional candour. | Candour Source Layer | Candour duties differ by nation and role. |
| NICE shared decision making and medicines safety context | Shared-decision-making workflow, medicines/prescribing context, and recording of risks, alternatives, preferences, and medicine decisions. | NICE Shared Decision Making and Medicines Safety | Clinical guidance context, not a product conformance route. |
| Data protection and individual rights | UK GDPR / Data Protection Act 2018, subject access, accuracy, rectification, controller/processor accountability, and health-data rights. | Data Protection and Health-Record Rights | Does not by itself satisfy common law confidentiality, professional duties, or deceased-record access. |
| DSA and DPIA | Deployment-specific data-sharing, lawful-processing, data-flow, controller/processor, confidentiality, transparency, retention, and subject-rights artefacts. | Data Protection and Health-Record Rights | A signed DSA or DPIA supports information-governance readiness only for its stated scope and date; it is not DSIC, GP Connect, or clinical-safety proof. |
| Records management and amendment practice | Retention, disposal, archive, legal hold, migration, correction, annotation, access-route separation, and nation-specific records codes. | Records Management and Amendment Practice | Needs local policy and record-type mapping. |
| PRSB and provenance | Record-content standards, Core Information Standard, provenance, implementation support, and conformance context. | PRSB Standards | Product/deployment proof still needs certificate, scope, configuration, and customer artefacts. |
| NHS information standards | NHS Standards Directory, information standards, DAPB/DAB, SNOMED CT, GP Connect, MESH, ITK3, and related standards surfaces. | NHS Standards Directory and DHSC Standards Direction | Standards applicability is not supplier implementation proof. |
| Clinical safety DCB0129/DCB0160 | Supplier manufacture safety, deployment/use safety, hazard ownership, clinical safety officer roles, residual risk, and change control for health IT that can affect care. | Clinical Safety DCB0129 and DCB0160 | Clinical-safety evidence is standard, supplier, component, workflow, and deployment specific. |
| Public records and access routes | Public records, archive/transfer, AHRA, FOI/EIR, AMRA, deceased-record access, and route separation. | UK Healthcare Recording Legal and Professional Position | Public-records and access law are not interchangeable routes. |
Project-Wide Link Rule
When a source-layer label appears in a visible synthesis table, link it to its canonical page or section. Create a new page only when the label is repeated, decision-relevant, or needed to explain a source boundary that would otherwise be opaque.
Do not create a page for every source ID. Source IDs belong in Sources. Source-layer pages exist to explain a reusable evidence layer and to route readers to the correct canonical synthesis.