Digitize preparation, standardization, approval, traceability, and expiry control of all laboratory solutions in one GMP-compliant platform.
Zentixs Solution Management digitizes thecomplete lifecycle complete lifecycle of laboratory solutions—from preparation and standardization to approval, issuance, and disposal. Ensure complete lifecycle GMP compliance, complete lifecycle complete traceability, and complete lifecycle streamlined QC workflows through a secure, paperless platform.
Prepare and manage volumetric solutions with standardized concentrations and complete traceability.
Maintain certified primary standards with approval workflows, expiry tracking and audit history.
Digitally control reagent preparation, inventory usage, issuance and lifecycle management.
Create validated buffer preparations with automated calculations and GMP compliance.
Prepare HPLC and analytical mobile phases using controlled workflows and electronic approvals.
Manage titrants and microbiological media with complete preparation and usage history.
From request to disposal — every action recorded, approved, and audit-ready.
Create solution requests, follow SOP-based preparation templates, and auto-calculate formulas and batch quantities.
Purpose-built for pharmaceutical QC — every feature maps directly to a GMP requirement or lab workflow need.
SOP-based templates with auto formula and batch calculations — no manual errors.
Multi-trial potency factor calculation against primary standards with acceptance criteria.
Auto-generate GMP barcode and QR labels with solution ID, expiry, and storage details.
21 CFR Part 11-compliant e-signatures at every approval step with full identity audit.
Configurable analyst → supervisor → QA chain with email alerts and rejection handling.
Real-time issued, consumed, and remaining quantities with low-stock and reorder alerts.
Automated near-expiry alerts, auto-block of expired solutions, and extension workflows.
Link every solution use to sample, batch, test, instrument, analyst, and date.
Every action time-stamped and user-attributed. Fully searchable and export-ready.
200+ pharmaceutical and biotech QC laboratories rely on Zentixs Solab to eliminate paper registers, prevent compliance gaps, and keep every solution traceable.
Eliminate paper solution registers entirely. Every record is digital, searchable, and instantly accessible.
Auto-calculated potency, factor, and batch formulas. Standardization against approved primary standards.
Proactive expiry alerts and auto-block prevent expired solutions from reaching analysts.
Complete solution history and audit trail accessible in one click — always audit-ready.
Digital SOPs, auto labels, and streamlined approval workflows cut lab cycle times significantly.
Designed to satisfy FDA, WHO, and EU regulatory expectations out of the box.
Every record in Solab is attributable, legible, contemporaneous, original, and accurate. ALCOA+ data integrity is enforced by design — not by policy.
Immutable audit trail on every action
Role-based access with electronic signature controls
Full IQ/OQ/PQ validation documentation package
Automated deviation & CAPA tracking
Complete solution history — always inspection-ready
Electronic records & e-signatures
Computerised systems validation
Pharmaceutical inspection cooperation
US FDA data integrity guidelines
Data integrity principles
World Health Organization
Built from the ground up to meet pharmaceutical industry standards — not retrofitted.
Enterprise-grade security to protect your critical data.
Role-based access control
Multi-factor authentication support
Encrypted data at rest and in transit
Session management & access logs
Validation-ready by design with complete documentation and control.
Full IQ/OQ/PQ documentation package
GAMP 5 Category 4/5 classification
Change control & version management
Validation protocols included
Aligned with global regulatory standards and best practices.
21 CFR Part 11 electronic signatures
EU Annex 11 system controls
ALCOA+ data integrity by design
WHO GMP & PIC/S compliant
Zentix Solab is engineered for compliance, trusted for integrity, and built to support quality at every step.
Solab connects seamlessly with the tools your lab already uses — no silos, no duplicate data entry.
Core lab information management
Sample registration & tracking
Reagent & material stock control
Equipment calibration & status
Electronic lab notebook entries
Scientific data management
Certificate of analysis generation
SOP & controlled document storage