Quality Assurance (QA)
Route potency, pesticide residue, heavy metal, and microbial test results through configurable multi-level QA approval workflows, ensuring every certificate of analysis (COA) is reviewed and signed off before it reaches the client.
Quality Control (QC)
Build QC checks — blanks, duplicates, spikes, and reference standards — directly into your test methods, and let Revol LIMS automatically flag out-of-specification results before a batch is released.
Trend Analysis
Monitor instrument performance, analyst performance, and QC outcomes over time using built-in trend charts and control limits, so labs can catch drift early and act before it becomes a non-conformance.
Instrument Calibration & Maintenance
Schedule, track, and document calibration and preventive maintenance for every analytical instrument — HPLC, GC-MS, balances, pipettes — with automated reminders that keep your lab audit-ready year-round.
Document Management
Maintain version-controlled SOPs, methods, and quality records with full revision history, electronic sign-off, and controlled distribution — satisfying ISO 17025 documentation and record-control requirements without manual file tracking.
Non-Conformance and CAPA Management
Non-Conformance & CAPA Management — Log non-conformances the moment they're identified, link them directly to the affected samples or batches, and manage corrective and preventive actions through to closure within a single auditable record.