TEKLYNX CENTRAL is a centralized label management solution for label design, approval, printing, and reporting, increasing operational efficiency.
Vendor
TEKLYNX
Company Website
TEKLYNX CENTRAL is an all-in-one labeling solution designed to manage the entire labeling process centrally. It combines label design, traceability, and print automation. This software is particularly beneficial for organizations with complex labeling requirements, enabling them to manage supply chain labeling and integrate with ERP and other business systems. It allows users to print labels from anywhere using a browser-based interface and manage an unlimited number of printers from a single server, whether on-premise or in the cloud. The software provides complete version history and audit trails throughout a label's lifecycle. System administrators can coordinate licensing and define system-wide settings in a single location, rolling them out across the entire global organization. Browser-based access eliminates the need for individual workstation installations, reducing system maintenance and software upgrade costs. TEKLYNX CENTRAL helps to reduce errors and misprints through a customizable user interface. It simplifies complex printing processes into easy-to-master steps, allowing for the creation of separate processes tailored to the needs of each department, business unit, supplier, or vendor. The controlled labeling environment ensures security and accuracy by enforcing defined business processes at every level, restricting access to only the printers, labels, and tasks a user needs to perform their job. It also maintains a High-Availability (HA) environment with intuitive automatic back-up server functionality. The software is built to integrate with SAP, Oracle, and other ERP systems, avoiding complex and costly custom development and eliminating compatibility issues. TEKLYNX CENTRAL also aids in compliance with industry standards such as GHS and CFR. For GHS compliance, it can pull symbols, signal words, and hazard elements from a centralized database. For CFR compliance, it helps address FDA regulatory compliance standards such as 21 CFR Part 11, using electronic signatures linked to relevant records. The Validation Accelerator Pack (VAP) includes templates that outline acceptance criteria, testing instructions, expected results, and worksheets for documenting testing results, accelerating the validation of labeling processes.
Features
- Centralized Label Management
- System administrators can coordinate licensing and define system-wide settings in a single location, rolling them out across the entire global organization.
- Manage unlimited printers from a single server, on-premise or in the cloud.
- System administrators can coordinate licensing and define system-wide settings in a single location, rolling them out across the entire global organization.
- Error Reduction
- A customizable user interface reduces errors and misprints, simplifying complex printing processes.
- Create separate processes tailored to the needs of each department, business unit, supplier, or vendor.
- A customizable user interface reduces errors and misprints, simplifying complex printing processes.
- Security and Accuracy
- A controlled labeling environment ensures security and accuracy by enforcing defined business processes at every level.
- Restrict access to only the printers, labels, and tasks a user needs to perform their job.
- Maintain a High-Availability (HA) environment with intuitive automatic back-up server functionality.
- A controlled labeling environment ensures security and accuracy by enforcing defined business processes at every level.
- ERP Integration
- TEKLYNX CENTRAL integrates with SAP, Oracle, and other ERP systems, avoiding complex and costly custom development.
- Eliminate compatibility issues.
- TEKLYNX CENTRAL integrates with SAP, Oracle, and other ERP systems, avoiding complex and costly custom development.
- Compliance
- Aids in compliance with industry standards such as GHS and CFR.
- Pull symbols, signal words, and hazard elements from a centralized database for GHS compliance.
- Helps address FDA regulatory compliance standards such as 21 CFR Part 11 for CFR compliance.
- Aids in compliance with industry standards such as GHS and CFR.