: Compliance

VERIXOR is an ERP system designed specifically for pharmaceutical companies. It helps manage formulations, R&D, batch production, quality checks, traceability, planning, warehousing, costing, and more—while staying compliant with FDA, cGMP, and 21 CFR Part 11 requirements.

VERIXOR supports regulated manufacturing with features like electronic records and signatures (21 CFR Part 11), audit trails, CAPA, non-conformance tracking, SOP control, BMR/MBR records, COAs, supplier management, and complete lot traceability—aligned with FDA and GxP expectations.

Yes. VERIXOR allows you to log non-conformance issues, manage CAPA workflows, track quality actions, and perform quality or stability testing as part of your batch and quality management processes.

VERIXOR provides secure formula management with version control, approval workflows, templates for dosage forms like capsules or softgels, label-claim tracking, formula comparison, batch scaling, physical property management, and BOM support for batch and packaged products.

Yes. VERIXOR tracks lots and expiry dates, enforces FEFO, manages quarantine and release processes, mandates SOP and QC checks, maintains full audit trails, and controls lot movement based on quality status.