Insights on batch record review, deviation management, 21 CFR Part 11 compliance, and how AI is changing pharmaceutical manufacturing quality.
DART was built for a different era of pharmaceutical QC. Modern QC teams need AI that reads, flags, and recommends — not just stores. Here's what to look for when evaluating DART alternatives in 2026.
Manual batch record review takes 4–8 hours per batch. AI cuts it to under 30 minutes. Here's how automated batch record review actually works — and what to look for in a solution.
What 21 CFR Part 11 actually requires for electronic batch records — audit trails, electronic signatures, access controls, and the compliance gaps most pharma companies miss.
Manual batch record review takes 4–8 hours per batch. Here's the exact approach to automate it while keeping 21 CFR Part 11 intact — AI does the data work, your QA team keeps the final call.
Watch an AI review a real pharmaceutical batch record — flagging deviations, citing 21 CFR requirements, and generating audit-ready documentation in under 30 minutes.
Watch the Demo →