The Reference Architecture for AI Agents in Regulated Life Sciences
The 7-layer reference architecture that turns individual AI compliance components into one integrated, inspectable, FDA-defensible system — from identity to evals.
Read Article →One conversational AI interface connecting specialized agents for SOP drafting, audit readiness, CSV, and 21 CFR Part 11 compliance.
Saram ConsultingThoughts and strategies on the intersection of Biotech, Artificial Intelligence, and Regulatory Compliance.
The 7-layer reference architecture that turns individual AI compliance components into one integrated, inspectable, FDA-defensible system — from identity to evals.
Read Article →How to build deterministic evaluation systems for AI agents in GxP computer system validation — code evaluators, narrow judges, binary metrics, and datasets that survive FDA inspection.
Read Article →A deep technical reference for building the deterministic control layer that makes AI agents inspectable, auditable, and defensible in FDA-regulated life sciences environments.
Read Article →A comprehensive engineering and governance playbook for deploying agentic AI in GxP environments — risk tiering, GAMP 5 validation, ALCOA+ audit trails, and the anti-patterns that get 483s.
Read Article →The hallucination war has shifted from 'build better models' to 'build better systems.' Here's what OpenAI, Anthropic, DeepMind, Meta, and xAI are actually doing — and why none of it will reach zero.
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