F
licenseNot graded
qualityD
maintenanceEnables AI agents to access FDA and ClinicalTrials.gov data for medical device compliance, adverse event monitoring, and regulatory due diligence.
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pharma-assistant-mcp
by Tangyufei233
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TDQS
C2.7/5.0
Scored across 2 tools
Disambiguation5/5
The two tools have clearly distinct purposes: one initiates a research process and returns its status, the other retrieves evidence metadata. No overlap in functionality.
Naming Consistency5/5
Both tool names follow a consistent verb_noun pattern in snake_case (run_research_intelligence, get_finding_evidence), which is clear and predictable.
Tool Count2/5
With only 2 tools for a pharmaceutical assistant, the tool surface is extremely thin. A typical assistant for this domain would require many more tools for tasks like drug lookup, adverse event reporting, and clinical trial management.
Completeness2/5
The tool set covers only initiating research and viewing evidence metadata, missing essential operations such as creating/updating/deleting findings, searching existing data, or managing workflows. The surface feels incomplete for the stated domain.
Maintenance
ActivityMaintained
ResponsivenessSyncing