Scispot Connector for AI agents.

Yes. The Scispot MCP allows you to pull full audit logs and operation histories instantly. This makes it much easier to demonstrate data integrity and keep your documentation ready for regulatory inspections.

It provides a direct line to your sample database. You can ask your agent to check the status of any sample, see its current testing phase, or view its chain of custody details without opening the LIMS.

Absolutely. You can query the status of all your laboratory instruments to see which are active, which are offline, and when their next calibration or maintenance is scheduled.

Yes. You can ask your agent to list all pending CoAs or pull specific ones for your clients, including potency profiles and contaminant screening results.

It gives you a bird's-eye view of your operations. You can quickly identify bottlenecks in sample intake, monitor rush orders, and see which batches are ready for release.

Yes. It allows you to link samples directly to production batches, providing full traceability for your seed-to-sale tracking and compliance reporting.

Yes. You can query your client list and ask for the status of their specific orders to get real-time updates on test results and estimated completion dates.

Yes! Use the list_results capability to fetch all completed analytical findings for a specific sample. Your AI agent will respond with comprehensive pass/fail determinations across potency, terpenes, pesticides, heavy metals, mycotoxins, and microbial panels. Once all state-mandated tests show passing results, use list_certificates to verify CoA generation status and confirm automatic Metrc submission. Always verify regulatory limit compliance before releasing products to distribution or retail channels.

Simply ask the agent to run the list_instruments action. It will compile all analytical equipment tracked via Scispot GLUE integration with calibration status, last service date, next scheduled maintenance, IQ/OQ/PQ qualification records, and current operational state. The AI will proactively highlight any HPLC, GC-MS, ICP-MS, or other systems approaching calibration expiry or overdue for preventive maintenance. This ensures your laboratory maintains ISO/IEC 17025 compliance, analytical data integrity, and inspection readiness at all times.

No. The current toolset focuses strictly on read-only querying and analytical operations. listing samples, reviewing results, checking certificates, monitoring workflows, and tracking instrument health. State alteration operations (modifying test data, deleting samples, revoking certificates, or changing approvals) are not currently exposed. This design assures your laboratory records remain secure against destructive queries, maintains complete audit trail integrity for regulatory inspections, and preserves data immutability required by FDA 21 CFR Part 11 and ISO/IEC 17025 standards.