FDA regulatory consultant for medical device companies. Provides 510(k)/PMA/De Novo pathway guidance, QSR (21 CFR 820) compliance, HIPAA assessments, and dev...
Trades Polymarket prediction markets on FDA drug approvals, biotech IPOs, clinical trial outcomes, pharma M&A, and precision medicine milestones. Use when yo...
Provide seamless access to comprehensive FDA drug data through intuitive search and detailed information retrieval. Enable discovery of drugs by name, indication, similarity, and application history t
Senior Regulatory Affairs Manager for HealthTech and MedTech companies. Prepares FDA 510(k), De Novo, and PMA submission packages; analyzes regulatory pathwa...
Provide comprehensive and authoritative medical information by querying multiple trusted sources including FDA, WHO, PubMed, RxNorm, and Google Scholar. Enable detailed drug data retrieval, health sta
Search NHTSA vehicle recalls, FDA food/drug recalls, and CFPB consumer complaints. 3 tools for product safety monitoring.
The first financial intelligence MCP server. Live AI-scored trading signals from Reddit, SEC filings, FDA approvals, Congressional trades, and 15+ sources. 7 tools, 2 resources, hosted remotely, free,
Monitor and analyze market-moving catalysts including earnings, FDA decisions, economic data releases, and corporate events
Fetches and analyzes FAERS (FDA Adverse Event Reporting System) data from openFDA API. Supports drug names and SMILES (resolves via PubChem). Generates: even...
Assist businesses in developing, auditing, and maintaining HACCP plans and FDA/USDA food safety programs for hazard control and regulatory compliance.
Generate professional labels in LMP format from natural language descriptions, with optional one-click preview link (no API key required)
Document control system management for medical device QMS. Covers document numbering, version control, change management, and 21 CFR Part 11 compliance. Use...
Curated skill bundle for medical device companies, digital health startups and pharma R&D teams. Activates the firm pyramid with RA (Regulatory Affairs), Cli...
Determine whether an incident in a clinical trial is a "major deviation" or "minor deviation". Function: Automatically classify protocol deviations in clinic...
CAPA system management for medical device QMS. Covers root cause analysis, corrective action planning, effectiveness verification, and CAPA metrics. Use for...
Senior Quality Manager Responsible Person (QMR) for HealthTech and MedTech companies. Provides quality system governance, management review leadership, regul...
Conduct security audits for OpenClaw-based AI assistants on macOS to detect exposure risks, weak tokens, sensitive commands, and IP leaks.
Intelligent Triage and Symptom Analysis Skill. Supports 650+ symptoms across 11 body systems. Based on ESI and Manchester Triage System with 5-level triage c...
Fetch iMessage/Messages.app attachments (voice memos and images) and process them — transcribe audio via Silicon Flow ASR (SenseVoiceSmall), and analyze imag...
Evaluate and improve your organization's data governance across six domains by scoring controls, identifying risks, and prioritizing remediation actions.