Firm Medtech Pack

Curated skill bundle for medical device companies, digital health startups and pharma R&D teams. Activates the firm pyramid with RA (Regulatory Affairs), Clinical, R&D and Quality agents pre-configured for FDA/CE compliance, clinical documentation and pharmacovigilance workflows.

Sector bundle for medical technology & digital health environments.

Activated departments

Department	Services activated	Focus
RA	Regulatory Affairs · Compliance Legal	FDA 510(k), CE Marking, MDR
Research Development	Research Discovery · R&D Prototyping	Clinical evidence, biomarker research
Quality	Compliance Auditing · Reliability · Security	ISO 13485, IEC 62304
Legal	Privacy/Data Protection · IP	HIPAA, patient data, patents
Operations	Documentation · SRE/Incident	DHF, adverse event reporting

Recommended ClawHub skills to install alongside

bash

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

Firm configuration overlay

json

{
  "agent": {
    "model": "anthropic/claude-opus-4-6",
    "workspace": "~/.openclaw/workspace/medtech-firm"
  },
  "agents": {
    "defaults": {
      "sandbox": { "mode": "non-main" }
    }
  }
}

Prompt: regulatory submission prep

text

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"

Prompt: adverse event review

text

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"

Regulatory coverage

Standard	Department	Service
FDA 510(k) / PMA	RA	Regulatory Affairs
EU MDR 2017/745	RA + Legal	Regulatory + Privacy
ISO 13485:2016	Quality	Compliance Auditing
IEC 62304	Engineering	AI Engineering
HIPAA	Legal	Privacy/Data Protection
21 CFR Part 11	Quality	Security
ISO 14971	RA + Quality	Risk Management

Security notes

• 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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