Requirements
- Target platform
- OpenClaw
- Install method
- Manual import
- Extraction
- Extract archive
- Prerequisites
- OpenClaw
- Primary doc
- SKILL.md
Curated skill bundle for medical device companies, digital health startups and pharma R&D teams. Activates the firm pyramid with RA (Regulatory Affairs), Cli...
Curated skill bundle for medical device companies, digital health startups and pharma R&D teams. Activates the firm pyramid with RA (Regulatory Affairs), Cli...
Hand the extracted package to your coding agent with a concrete install brief instead of figuring it out manually.
I downloaded a skill package from Yavira. Read SKILL.md from the extracted folder and install it by following the included instructions. Tell me what you changed and call out any manual steps you could not complete.
I downloaded an updated skill package from Yavira. Read SKILL.md from the extracted folder, compare it with my current installation, and upgrade it while preserving any custom configuration unless the package docs explicitly say otherwise. Summarize what changed and any follow-up checks I should run.
Sector bundle for medical technology & digital health environments.
DepartmentServices activatedFocusRARegulatory Affairs Β· Compliance LegalFDA 510(k), CE Marking, MDRResearch DevelopmentResearch Discovery Β· R&D PrototypingClinical evidence, biomarker researchQualityCompliance Auditing Β· Reliability Β· SecurityISO 13485, IEC 62304LegalPrivacy/Data Protection Β· IPHIPAA, patient data, patentsOperationsDocumentation Β· SRE/IncidentDHF, adverse event reporting
npx clawhub@latest install academic-research # PubMed / clinical trial search npx clawhub@latest install admet-prediction # Drug candidate ADMET analysis npx clawhub@latest install pdf-documents # Clinical study PDF parsing npx clawhub@latest install arc-security-audit # 21 CFR Part 11 audit trail npx clawhub@latest install firm-orchestration # A2A orchestration backbone
{ "agent": { "model": "anthropic/claude-opus-4-6", "workspace": "~/.openclaw/workspace/medtech-firm" }, "agents": { "defaults": { "sandbox": { "mode": "non-main" } } } }
Use firm-orchestration with: objective: "Prepare 510(k) substantial equivalence summary for continuous glucose monitor" departments: ["ra", "research_development", "quality"] constraints: ["FDA guidance K020431 reference", "predicate device: Dexcom G6"] definition_of_done: "510(k) summary draft with predicate comparison table" delivery_format: "structured_document"
Use firm-orchestration with: objective: "Classify and triage Q4 adverse event reports against MDR Art. 87" departments: ["ra", "quality", "legal"] constraints: ["read-only access", "anonymize patient identifiers in output"] definition_of_done: "Triage matrix with reportability decisions per event" delivery_format: "markdown_report"
StandardDepartmentServiceFDA 510(k) / PMARARegulatory AffairsEU MDR 2017/745RA + LegalRegulatory + PrivacyISO 13485:2016QualityCompliance AuditingIEC 62304EngineeringAI EngineeringHIPAALegalPrivacy/Data Protection21 CFR Part 11QualitySecurityISO 14971RA + QualityRisk Management
PHI (Protected Health Information): SECURE_PRODUCTION_MODE=true mandatory All outputs must be anonymized: enforce via POLICY_BLOCKED_TOOLS for export Audit trail required by 21 CFR Part 11: AUDIT_ENABLED=true
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Code helpers, APIs, CLIs, browser automation, testing, and developer operations.
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