Precision measurement and quality control software
VeriGage helps manufacturers improve consistency, maintain compliance, and ensure confidence in every measurement.
The Quality of Your Calibration Management Software Matters
Because your reputation—and your products—depend on it.
VeriGage helps manufacturers improve consistency, maintain compliance, and ensure confidence in every measurement. It's trusted by quality teams and respected by auditors for delivering reliable calibration management with clarity and control.
Don't risk the integrity of your products with unreliable tools.
Choose VeriGage—where precision meets performance.
Why Teams Choose VeriGage
- Reduce Downtime
Stay on schedule with real-time calibration tracking and alerts
- Control Costs
Focus resources where they're needed and avoid unnecessary calibrations
- Ensure Compliance
Designed to support international standards, including FDA and ISO
- Simplify Audits
Keep clear records and traceability throughout the calibration lifecycle
Powerful Tools, Built-In
VeriGage provides everything you need in one system:
- Asset and gauge management
- Scheduled and ad-hoc calibrations
- Printable calibration certificates and barcoded labels
- Gage R&R studies (MSA, 4th Edition)
- Full audit trail and reporting tools
- Straightforward, user-friendly interface
Experience the VeriGage difference.
Better quality starts with better calibration software.
Comprehensive Software Modules
VeriGage offers a complete suite of integrated screens and modules to manage every aspect of your quality control process.
Scheduling
The All Gage Schedules Due screen shows all of your calibrations, gage reminders, gage activities and MSA studies due so that you can see your entire schedule at a glance or narrow it down by schedule type. Listings are easily output to email either manually or on a predefined schedule.
Calibrations
VeriGage maintains a complete, detailed history of all your calibrations and will track and monitor the cost of failed calibrations. It also includes comprehensive calibration frequency adjustment tools to monitor and automatically adjust calibration frequencies based on common NCSL performance guidelines.
Calendar
VeriGage's comprehensive calendar-based scheduling lets you establish schedules for your calibrations, activities, MSA studies, transfers and reminders. Conflicts are easy to remedy with simple, drag-and-drop functionality.
Crib
VeriGage includes comprehensive crib management. Transfers can follow two-step transactional or single-step routing models; transfer a single gage or multiple gages in a batch and apply configurable routing rules to fit your needs.
Reporting
Conveniently generate ad-hoc and canned reports from relevant areas of the program. The intuitive navigation displays the report preview next to your current master tabs, so you can easily cross-compare results with live data. With just a few clicks, you can import, export, save and email reports.
Calibrations Due
This screen shows a list of all calibrations coming due and can be sorted, filtered, printed or exported as needed. Additionally, you can set up automatic email notifications for gages coming due.
Advanced Modules
Extend VeriGage's capabilities with these powerful add-on modules
Info Center
A window into your quality system is a window of opportunity.
Use VeriGage Info Center to ensure calibrations are being completed on time, verify that gages coming due are never overlooked and so much more. This efficient on-demand reporting utility is a must-have asset in your quest for continuous improvement.
Calibration Label Printer
Create durable, laminated, bar-coded calibration labels directly out of VeriGage to minimize mistakes and reduce costs.
This compact Brother® printer (PT-P900WC desktop or PT-P950NW network) comes with cables and a starter label cartridge. The harsh-environment labels are available in a variety of sizes and colors.
Crib
With VeriGage Crib, you'll never lose track of your gages again.
VeriGage Crib is an extensive crib management tool. Transfers can follow two-step transactional or single-step routing models; transfer a single gage or multiple gages in a batch and apply configurable routing rules to fit your needs.
Procedures
Import any or all procedures into VeriGage using the provided import utility or print them as hard copy from the included PDF file. You can also use CalPro as a library of work instructions for inclusion within your company's Quality Manual.
FDA Compliance Manager
This software and our onsite validation services ensure preparedness for successful future audits.
VeriGage's FDA Compliance Manager will assist you in managing your organization's ongoing FDA compliance requirements. In FDA Mode, this module will ensure that the specific functionality required to meet FDA 21 CFR Part 11 is enforced.
Key Features
VeriGage offers a comprehensive set of features designed to streamline your measurement and quality control processes.
Real-time Measurement
Collect and analyze measurement data in real-time from CMMs, calipers, micrometers, and other measurement devices.
Statistical Process Control
Monitor and control your manufacturing processes with comprehensive SPC tools, including control charts and capability analysis.
Customizable Dashboards
Create personalized dashboards to visualize the metrics that matter most to your operation, with drag-and-drop simplicity.
Compliance Management
Ensure compliance with industry standards like ISO 9001, IATF 16949, and AS9100 with built-in documentation and audit trails.
Device Integration
Seamlessly connect with a wide range of measurement devices from leading manufacturers, with plug-and-play simplicity.
Automated Alerts
Receive instant notifications when measurements fall outside of specified tolerances, allowing for immediate corrective action.
Why Choose VeriGage
VeriGage delivers tangible benefits that help manufacturers improve quality, reduce costs, and increase efficiency.
Reduce Defects by up to 35%
Early detection of process variations allows for immediate corrective action, significantly reducing defect rates.
Decrease Inspection Time by 50%
Automated data collection and analysis eliminates manual recording and calculation, freeing up valuable time.
Improve Traceability
Comprehensive audit trails and documentation ensure complete traceability for regulatory compliance and customer requirements.
Enhance Decision Making
Real-time data and analytics provide actionable insights, enabling informed decisions that drive continuous improvement.
Standards and Compliance
Achieve and maintain compliance with worldwide quality standards through systematic, adaptable, and auditable record keeping.
ISO 9001:2015
The ISO 9000 family of international quality management standards and guidelines has earned a global reputation as the basis for establishing quality management systems. VeriGage is specifically designed to help you gain control of your calibration management system and to assist you in maintaining compliance with the relevant sections of the ISO 9001:2015 standard.
Key sections supported:
- 7.1.5 Monitoring and Measuring Resources
IATF 16949:2016
IATF 16949:2016 (replacing the ISO/TS 16949:2009) is aligned with and refers to the most recent version of ISO's quality management systems standard, ISO 9001:2015, fully respecting its structure and requirements. IATF 16949:2016 is not a standalone quality management standard, but is implemented as a supplement to, and in conjunction with, ISO 9001:2015. VeriGage is specifically designed to help you gain control of your calibration management system and to assist you in maintaining compliance with the relevant sections of the ISO 9001 and IATF 16949:2016 standards.
ISO 13485:2016
This international standard specifies requirements for a quality management system where an organization needs to demonstrate its ability to provide medical devices and related services that consistently meet customer requirements and regulatory requirements applicable to medical devices and related services.
The primary objective of this international standard is to facilitate harmonized medical device regulatory requirements for quality management systems. As a result, it includes some particular requirements for medical devices and excludes some of the requirements of ISO 9001 that are not appropriate as regulatory requirements. VeriGage is specifically designed to help you gain control of your calibration management system and to assist you in maintaining compliance with the relevant sections of the ISO 9001 and ISO 13485 standards.
Key sections supported:
- 6.3 Infrastructure
- 7.5.6 Validation of processes for production and service provision
- 7.6 Control of monitoring and measuring equipment
- 8.5.2 Corrective action
- 8.5.3 Preventative action
ISO/IEC 17025:2017
This international standard is for use by laboratories in developing their quality, administrative and technical systems that govern their operations. Laboratory clients, regulatory authorities and accreditation bodies such as A2LA may also use it in conforming or recognizing the competence of laboratories. VeriGage is specifically designed to help you gain control of your calibration management system and to assist you in maintaining compliance with the relevant sections of the ISO 9001 and ISO/IEC 17025 standards.
Key sections supported:
- 6.4 Equipment
- 6.5 Metrological traceability
- 7.4 Handling of test or calibration items
- 7.5 Technical records
- 7.6 Evaluation of measurement uncertainty
- 7.7 Ensuring the validity of results
- 7.8 Reporting of results
- 7.11 Control of data and information management
AS9100 & AS13100
AS9100 is a widely adopted and standardized quality management system for the aerospace industry. It was released in October 1999 by the Society of Automotive Engineers and the European Association of Aerospace Industries.
AS9100 replaces the earlier AS9000 and the current revision (Revision D), includes the full text of the ISO 9001:2015, ensuring that the structure of the aviation, space and defense requirements align with the structure of ISO 9001:2015. VeriGage is specifically designed to help you gain control of your calibration management system and to assist you in maintaining compliance with the relevant sections of ISO 9001 and the AS9100 standards.
AS13100 has been created by the SAE G-22 Aerospace Engine Supplier Quality (AESQ) Technical Committee to harmonize and simplify supplier quality requirements that are in addition to the requirements of 9100 Quality Management Systems – Requirements for Aviation, Space, and Defense Organizations and 9145 Advanced Product Quality Planning and Production Part Approval Process.
Previously the Aerospace Engine Manufacturers based their supplier quality requirements on 9100 but had differing supplemental requirements and guidance albeit with largely the same intent. These supplemental requirements originate from the need to meet Regulatory, Customer, Industry, and Business requirements that are not explicitly covered by 9100 and 9145.
Key sections supported:
- 7.1.5 Monitoring and Measuring Resources
FDA 21 CFR Part 11 & 820
21 CFR Part 11 sets forth the FDA's standard for electronic signatures and tracking of all changes to your database. Companies that wish to have electronic records and electronic signatures accepted as equivalent to the corresponding paper records must comply with this standard.
To assure our customers of compliance with 21 CFR Part 11, CyberMetrics voluntarily undergoes independent 3rd party audit, review and certification. This includes actual on-site inspection of our records, product development practices, testing methods, maintenance procedure as well as specific functional assessment of our software.
The 21 CFR Part 11-compliant version of VeriGage permanently and automatically enables security and the Electronic Signature and Audit Trail features:
- Security: With security enabled, a user's access to forms can be limited; for instance, a user can have read-only access in Gage Entry (or no access at all), but can have full access to Calibration Entry in order to create calibration records.
- Electronic Signatures and Approvals: The 21 CFR Part 11-compliant version of VeriGage records signatures and approval signatures when calibrations are completed. Once a record is signed, it cannot be modified unless the original signer unsigns it.
- Audit Trail: The 21 CFR Part 11-compliant version of VeriGage automatically enables and indefinitely preserves the Audit Trail which maintains a comprehensive history of all user actions.
21 CFR Part 820 quality system regulation establishes the current good manufacturing practice (CGMP) requirements that govern the methods used, and the facilities and controls used for the design, manufacture, packaging, labeling, storage, installation and servicing of all finished devices intended for human use. VeriGage has been designed to comply with all relevant sections of Subpart G, 820.72 Inspection, Measuring, and Test Equipment.
FIPS
Federal Information Processing Standards (FIPS) are publicly announced standards developed by the United States federal government for use in computer systems by non-military government agencies and government contractors. VeriGage is designed to comply with FIPS standards for data security and encryption.