21 CFR Part 11 & ISO 17025 in Practice: What Your LIMS Must Actually Do
21 CFR Part 11 and ISO 17025, clause by clause: audit trails, e-signatures, document control, and what your LIMS must actually do.
August 27, 2026
Guide
From potency verification to contaminant screening, streamline your supplement testing workflows with automated compliance documentation and cGMP-ready reporting.
Automate potency, identity, and purity workflows from intake to certificate of analysis
Audit trails for cGMP, FDA DSHEA, and 21 CFR Part 111 — inspection-ready every day
Give supplement brands real-time access to potency results, COAs, and batch status

Quality Verification

Quality testing to verify product
specifications
Screening and quantification
for harmful substances

