Services
How we work with teams turning an assessment into action
Four formats — pick the one that fits where you are. Real prices, no contact-us-for-quote. Sign in to see the full scope, deliverables, and what we won't do.
AI Production Readiness Audit
You've built an AI prototype. Maybe with a consultancy, maybe in-house, maybe through an A4BEE Jumpstart. Two weeks tells you whether it's actually ready to run unsupervised in regulated production — and what it would cost to close the gap.
- Duration
- 2 weeks
- For
- Orgs with an existing AI deployment (prototype or production) who need an independent read on whether it's ready for regulated-industry production — or what it'll cost to get there
- Biotech
- Pharma
- Manufacturing
- AI
- Governance
- Strategy
AI Jumpstart for Biotech — fixed scope, fixed price
Two weeks. One biotech AI use case picked from a curated menu. One day of discovery workshop plus 80 hours of A4BEE engineering. Working prototype delivered at the end — not a slide deck, not a roadmap. Fixed price, day-one usable, regulatory-aware from the start.
- Duration
- 2 weeks end-to-end (1 day workshop + 80 hours engineering)
- For
- Biotech, pharma, or manufacturing org with one named AI use case and a sponsor ready to provide data + decisions for 2 weeks
- Biotech
- Pharma
- Manufacturing
- AI
- Automation
AI Operations Retainer
You shipped the AI. Keep it from drifting silently. Monthly retainer for orgs running RAG, agents, or LLM-backed workflows in regulated-industry production. Combines model + agent monitoring, drift detection, governance review, regulatory horizon scanning, and on-call escalation. Premium variant of the standard A4BEE retainer for AI-specific operations.
- Duration
- Rolling monthly, 60-day notice to terminate
- For
- Pharma + biotech + manufacturing orgs with AI / RAG / agentic systems running in regulated production — built by A4BEE or by anyone else
- Biotech
- Pharma
- Manufacturing
- AI
- Governance
GxP-Validated RAG Knowledge Assistant
A retrieval-augmented assistant for your SOPs, batch records, deviations, regulatory submissions — and the V-model validation file that lets you put it in production under GxP. Six to eight weeks. Working pipeline + the audit evidence package + the validation strategy.
- Duration
- 6–8 weeks depending on corpus complexity
- For
- Pharma + biotech orgs with 10k+ regulated documents (SOPs, batch records, deviations, CAPAs, submissions) and the operational appetite to use them via an AI assistant
- Biotech
- Pharma
- Manufacturing
- AI
- Data
- Governance
- Automation
Agentic AI for Biotech Operations
Multi-step AI agents that move work through your MES / LIMS / QMS instead of just answering questions about it. Wired into your operational systems via Anthropic MCP. Defined action envelope, named human-approval points, full audit trail. Built to survive a GxP inspection.
- Duration
- 10–14 weeks per agent (scope grows with integration count)
- For
- Pharma + biotech ops orgs with an integrated MES / LIMS / QMS estate and a named operational workflow they want to automate end-to-end
- Biotech
- Pharma
- Manufacturing
- AI
- Automation
- Governance