Every screen. Every button.
The complete user guide for Clarix — covering every workflow from receiving raw materials to releasing a batch, managing quality events, and preparing for an FDA inspection.
All modules
Getting Started
Dashboard, navigation, and your role in the system.
Batches
Create, execute, and release batch production records.
Formulas
Author and version master formula records with BOM and steps.
Inventory
Receive lots, track COA assay, FIFO issuance, and expiry alerts.
Quality
Deviations, RCIs, CAPAs, OOS, change control, and more.
Equipment
Asset registry, calibration logs, and PM schedules.
Environmental
ISO room sampling, excursion management, and T&H logging.
Training
Training plans, staff assignments, and the personnel matrix.
Reports
Yield, quality metrics, 483 readiness, EM trends, and more.
Administration
User management, organizations, and the audit trail.
Settings
Modules, numbering, e-signatures, business rules, and integrations.
Compliance
21 CFR Part 11, USP 797/cGMP, and e-signature audit guidance.
Labels
ZPL label templates for Zebra printers — batches and lot labels.
Documents
Controlled document library — SOPs, WIs, policies, and forms.
Facility
Floor plan, ISO-classified rooms, and equipment locations.
Lab
QC sample tracking and out-of-specification management.