Zentixs Vitara is a purpose-built digital platform designed to manage pharmaceutical reference standards, laboratory workflows, user roles, approvals, and compliance — all in one secure, audit-ready system.
Pharmaceutical laboratories struggle with complex challenges that manual systems can’t solve
Spreadsheets and paper logs create data silos and errors
Research and development reference standard tracking
CROs requiring compliant laboratory systems
Regulated manufacturing environments
Pharmaceutical laboratories face complex challenges that manual systems cannot efficiently solve.
Reduce time spent on manual processes and repetitive tracking.
Full GMP compliance with built-in audit readiness.
Eliminate manual tracking errors and improve operational accuracy.
Everything you need to manage pharmaceutical laboratory operations in one integrated platform
Controlled issuance workflow with complete audit trail from issuance to closure.
Role-based access with department-wise users and secure, controlled access.
Centralized Reports Center with system-generated audit trails for inspection readiness.
Version-controlled master data including pharmacopoeia, standard types, and storage conditions.
Track return, disposal, and wastage events with detailed usage logs.
Define dynamic attributes per standard with flexible data structure.
Configurable workflows for laboratory data closure, regulatory review, and QC/QA approvals.
Generate printable labels for standards and aliquots aligned with SOPs.
Import users, departments, standards via Excel with built-in validation.
Real-time overview of users, roles, departments, and standards with instant operational insights.
Create and manage Primary, Secondary, and Working Standards with full pharmacopoeia support.
Generate and track aliquots with unique numbers and batch-wise traceability.
Built from the ground up to support regulated pharmaceutical environments with complete audit readiness and data integrity
Comprehensive history of all changes
Encrypted and backed up automatically
Every action is logged and tracked
Role-based permissions and approvals
Data integrity at every level
Built for regulated pharmaceutical environments
Zentixs Vitara meets and exceeds the stringent requirements of global pharmaceutical regulatory bodies
Good Manufacturing Practice
FDA Compliance
Data Integrity
Quality Management
Audit-ready documentation and validation support included
Built for organizations that demand precision, compliance, and control
Complete quality control and assurance workflow management
Research and development reference standard tracking
CROs requiring compliant laboratory systems
Regulated manufacturing environments
Transform your laboratory operations with measurable improvements
Eliminate error-prone manual logs and paper-based systems
Close compliance gaps with complete traceability
Real-time insights across all lab operations
Eliminate error-prone manual logs and paper-based systems
Regulatory Compliance
