deepdna.aiVerified
Pharmacogenomics for AI agents: cited drug–gene, gene and rsID lookups plus a medication screen.
HealthcareData access / search
- Passed: Handshake
- Passed: Tools listed
- Passed: Updated recently
Median latency 1277 ms · Last checked
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Evidence for your next connection.
Independent measurements of remote MCP servers. Every observation has a timestamp.
Read-only probesMCP server · Data access / search
HealthGuard - 12-tool health/medical AI safety MCP: PII redaction, HIPAA, GDPR Art.9.
5 failed · 8 not measured
Median of successful probes over 7 days
Share of countable probes over 30 days, including daily rollups. Auth challenges are excluded.
Tool definitions returned by this server
Independent monitoring
Responded
The server completed its last measured handshake. This is an observation, not a guarantee.
Last checked| Test area | Passed | Failed | Unmeasured |
|---|---|---|---|
ConnectionCan a client connect and discover tools? | 4 | 1 | 0 |
Reliability & speedDoes it respond consistently and quickly? | 0 | 0 | 4 |
Access & authenticationWhat is required to use this server? | 1 | 0 | 2 |
Tool qualityAre the tool definitions usable by an agent? | 2 | 2 | 0 |
Publisher identityCan the publisher be traced to its source? | 2 | 2 | 2 |
Unmeasured means there is not enough evidence to decide. How these checks work
Start using io.tooloracle/healthguard
Choose your client, copy the configuration, then enable the server in your client’s MCP settings.
Run this command in your terminal, then restart Claude Code.
Claude Code
claude mcp add --transport http io-tooloracle-healthguard https://tooloracle.io/health/mcp/Capabilities
Generate pharmacovigilance adverse event report template (MedDRA). Includes EU/DE/US reporting obligations and deadlines.
DiscoveredClinical trial phase requirements under EU CTR 536/2014. Phase I-IV details, CTIS requirements, German specifics.
DiscoveredMDR Annex VIII medical device risk classification. Determines Class I/IIa/IIb/III based on device characteristics.
DiscoveredBasic drug-drug interaction risk check. Educational tool — not a clinical decision system. Checks known high-risk combinations.
DiscoveredGDPR Art.9 health data processing compliance assessment. Returns required legal basis, DPIA requirements, retention periods.
DiscoveredGood Manufacturing Practice (GMP) audit checklist per EU EudraLex Vol.4. QMS, personnel, premises, documentation, production, QC.
DiscoveredHIPAA vs GDPR comparison for healthcare organizations. Side-by-side analysis with dual-compliance tips.
DiscoveredICD-10 code lookup and search. Covers common codes and chapter overview. Uses ICD-10-GM (German Modification).
DiscoveredEU IVDR 2017/746 in-vitro diagnostic device compliance. Risk class A-D, Notified Body requirements, transition deadlines.
DiscoveredEU MDR 2017/745 compliance assessment for medical devices. Checks CE marking, Notified Body, Clinical Evaluation, PMS, UDI, QMS, EUDAMED. Returns compliance score.
DiscoveredEU healthcare regulatory deadlines. MDR/IVDR transitions, AI Act obligations, NIS2, PSUR deadlines.
DiscoveredValidate UDI (Unique Device Identification) format per MDR Art. 27. Identifies issuing agency (GS1/HIBCC/ICCBBA).
DiscoveredRecent measurements
| Checked | Result | Response | Tools |
|---|---|---|---|
| Connected | 87 ms | 12 |