For clinical researchers
Frame a research question, draft with specialist AI agents, arrange evidence on a chapter canvas and publish versioned papers, with the writer approving every change.
3
specialist research agents
4
citation styles supported
1
stable short link per paper
Research projects
Each paper starts from a research question that steers every chat and compile.
AI research agents
A research writer, a citation curator and a medical expert, each with a defined role.
Chapter canvas
Drag-and-drop snippets into chapters. Each snippet keeps its original text and where it came from.
Writing assistant
Suggested passages sit beside the manuscript and are only inserted when the writer approves them.
Compile & edit
Compile chapters into a manuscript, then edit it. The agent's original compile is kept for reference.
Versioned publishing
Publish fixed, numbered versions under one stable short link, ready to print or export to Word.
Database-centred by design
Every test, price, patient, order, result, role and region rule lives as a structured database record. No hard-coded catalogues, every change traceable.
Multi-tenant companies
Each practice, clinic or laboratory is its own tenant. Records are stamped with the tenant and checked server-side on every read and write.
Group hierarchy
Link sites under a parent organisation (hospital group or network) with roll-up visibility across its sites.
Layered user permissions
Owner, admin, manager and viewer roles, plus custom roles with per-module permissions, SSO (Microsoft / Google) and bulk user provisioning.
Privacy by design (GDPR)
Built to support UK/EU GDPR: patient-controlled access grants, recorded and withdrawable consent, private file storage and account deletion.
Audit and provenance
Access changes, clinical actions and AI extractions are logged with who, what and when, so every decision can be explained.
Hosted on Base44 infrastructure, which holds SOC 2 attestation at platform level. Clinarivo itself is not independently SOC 2 certified, and GDPR support describes design controls; each practice remains the data controller responsible for its own compliance.
Faster first drafts
Clear provenance for every passage
Writer stays in control
Vancouver, APA, Harvard or AMA references
Reference: frameworks that apply to users in each region. Not a claim of compliance.
| United Kingdom | United Arab Emirates | United States | |
|---|---|---|---|
| Data protection | UK GDPR & Data Protection Act 2018 | Federal PDPL (Decree-Law 45/2021) · ICT in Health Fields Law (Federal Law 2/2019) | HIPAA Privacy & Security Rules · HITECH Act |
| Regulators | CQC (care quality) · MHRA (devices & IVDs) · ICO (data) | MOHAP · DHA (Dubai) · DOH (Abu Dhabi) | HHS OCR (privacy) · CMS (CLIA) · FDA (devices & IVDs) |
| Lab quality | UKAS — ISO 15189 accreditation | ENAS — ISO 15189 accreditation | CLIA certification · CAP accreditation |
| Clinical reference | NICE guidelines · BNF formulary | MOHAP / DHA / DOH clinical standards | USPSTF · CDC · FDA labelling |
Reference: codes from these sources are stored on records. No live connection.
Capabilities listed are built into Clinarivo today. Regulatory frameworks and official databases are shown for orientation only: Clinarivo stores standard codes (SNOMED CT, LOINC, CPT, HCPCS, ICD-10) on records, but does not connect live to these databases and holds no certification. Each organisation remains responsible for its own regulatory compliance.
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Information only, not medical advice.