extract: 2026-01-16-nhs-england-ai-scribing-supplier-registry-19-vendors
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{
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"rejected_claims": [
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{
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"filename": "nhs-dtac-compliance-creates-indirect-forcing-function-for-clinical-ai-safety-transparency-through-mandatory-clinical-safety-case-disclosure.md",
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"issues": [
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"missing_attribution_extractor"
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]
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},
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{
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"filename": "openevidence-uk-expansion-requires-choice-between-formal-nhs-compliance-with-safety-disclosure-or-informal-individual-clinician-use-without-reimbursement.md",
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"issues": [
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"missing_attribution_extractor"
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]
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}
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],
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"validation_stats": {
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"total": 2,
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"kept": 0,
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"fixed": 6,
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"rejected": 2,
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"fixes_applied": [
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"nhs-dtac-compliance-creates-indirect-forcing-function-for-clinical-ai-safety-transparency-through-mandatory-clinical-safety-case-disclosure.md:set_created:2026-03-24",
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"nhs-dtac-compliance-creates-indirect-forcing-function-for-clinical-ai-safety-transparency-through-mandatory-clinical-safety-case-disclosure.md:stripped_wiki_link:healthcare-AI-regulation-needs-blank-sheet-redesign-because-",
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"nhs-dtac-compliance-creates-indirect-forcing-function-for-clinical-ai-safety-transparency-through-mandatory-clinical-safety-case-disclosure.md:stripped_wiki_link:OpenEvidence-became-the-fastest-adopted-clinical-technology-",
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"openevidence-uk-expansion-requires-choice-between-formal-nhs-compliance-with-safety-disclosure-or-informal-individual-clinician-use-without-reimbursement.md:set_created:2026-03-24",
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"openevidence-uk-expansion-requires-choice-between-formal-nhs-compliance-with-safety-disclosure-or-informal-individual-clinician-use-without-reimbursement.md:stripped_wiki_link:OpenEvidence-became-the-fastest-adopted-clinical-technology-",
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"openevidence-uk-expansion-requires-choice-between-formal-nhs-compliance-with-safety-disclosure-or-informal-individual-clinician-use-without-reimbursement.md:stripped_wiki_link:prescription-digital-therapeutics-failed-as-a-business-model"
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],
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"rejections": [
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"nhs-dtac-compliance-creates-indirect-forcing-function-for-clinical-ai-safety-transparency-through-mandatory-clinical-safety-case-disclosure.md:missing_attribution_extractor",
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"openevidence-uk-expansion-requires-choice-between-formal-nhs-compliance-with-safety-disclosure-or-informal-individual-clinician-use-without-reimbursement.md:missing_attribution_extractor"
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]
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},
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"model": "anthropic/claude-sonnet-4.5",
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"date": "2026-03-24"
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}
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@ -7,9 +7,13 @@ date: 2026-01-16
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domain: health
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secondary_domains: [ai-alignment]
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format: news
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status: unprocessed
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status: null-result
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priority: high
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tags: [nhs-dtac, clinical-ai-safety, regulatory-compliance, openevidence, ambient-scribing, mhra, supplier-registry, uk-healthcare, belief-5]
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processed_by: vida
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processed_date: 2026-03-24
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extraction_model: "anthropic/claude-sonnet-4.5"
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extraction_notes: "LLM returned 2 claims, 2 rejected by validator"
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---
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## Content
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@ -60,3 +64,15 @@ NHS England published a self-certified supplier registry for AI-enabled ambient
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PRIMARY CONNECTION: Session 11 regulatory track finding — NHS DTAC compliance is an observable forcing function
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WHY ARCHIVED: Provides concrete evidence that the NHS regulatory compliance mechanism is operational (19 vendors), and that OE is choosing not to comply despite clear competitive incentive
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EXTRACTION HINT: Focus on OE's conspicuous absence from registry + what DTAC compliance would require (clinical safety disclosure) — this is the structural gap claim
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## Key Facts
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- NHS England published AI scribing supplier registry on January 16, 2026
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- 19 vendors completed DTAC + MHRA Class 1 requirements by registry launch
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- Registry applications reopened February 3, 2026, remain open indefinitely
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- DTAC V2 published February 24, 2026 with 25% fewer questions
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- April 6, 2026 deadline: ALL NHS digital health procurement must use DTAC V2
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- NHS England April 2025 guidance mandates DCB0160, DPIA, MHRA determination, DTAC for AI scribing
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- OpenEvidence 'Visits' launched August 2025 as documentation + CDSS hybrid tool
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- OpenEvidence is not on the 19-vendor NHS registry as of January 2026
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- NHS DTAC requires DCB0160 clinical safety case including hazard identification, risk assessment, risk control measures, post-market surveillance
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