The AI kit for Laboratory managers

Builds reorder lists, expiry reports and stock audits, for example flagging 12 reagents expiring within 60 days.

Analyzes QC data and drafts SOPs, non-conformance reports and CAPA plans, for example investigating a control chart shift.

Creates equipment inventories and recurring maintenance calendars, for example a quarterly PM schedule for six centrifuges.

Improves protocols with troubleshooting steps and cost comparisons, for example cutting a digestion step from 4 hours to 2.

Like "Set Up Inventory Level Tracking"

Like "Chemical Inventory Management System"

Like "Data Cleaning and Quality Assurance"

Like "Analyze Equipment Downtime Data"

Every experiment starts with valid materials and bookings ready.

Feasible facility schedules that include every prerequisite.

Make sure everyone who performs a task has documented training on the current SOP version.

Keep shared instruments busy with ready samples in the order that best serves deadlines.

Let your AI search your Pinecone Assistant knowledge base and bring back answers with sources.

Let your AI search your Ragie knowledge base and pull back the right passages when you ask a question.

Search your own PDFs, EPUBs and Word files locally and get answers with page and section citations.

Search your own PDF, Word, text and Markdown files from your AI chat, all on your own computer.

Ascenscia is an AI voice assistant for scientific labs, offering 97% accuracy in recognizing scientific terms. It integrates seamlessly with lab software to ena

Knowledge Hub centralizes information, providing quick access to accurate data and insights. It streamlines research and decision-making by organizing knowledge

Pane is an AI spreadsheet that edits cells, writes real formulas, extracts tables from PDFs, cleans messy data and builds charts-so every change is visible, edi

Doclime lets you quickly find answers within your documents. Upload files and ask questions to receive instant, accurate responses with citations, saving time a

Build a searchable internal research library with project-aware permissions and document provenance, so audits trace every source.

Check protocol completeness and keep version history without inventing parameters, so technicians always work from the approved version.

Keep project decisions, tasks and updates in one owned workspace, so coordination overhead drops and nothing gets lost.

Equipment-specific context with evidence for investigation rather than automatic diagnosis.

Oversees quality system governance and regulatory compliance for HealthTech and MedTech companies.

Manages document control, change control, and regulatory documentation compliance for medical device organizations.

Manage non-conformance lifecycle, root cause analysis, and CAPA in regulated manufacturing.

Manages regulatory strategy and submissions for HealthTech and MedTech devices.