Document control
Manage revisions, reviews, approvals, access and complete document history.
Explore CIS document managementContinuous Improvement Software
CIS Software connects inspections, audits, document control, corrective actions, training, calibration, suppliers, production and reporting in one configurable platform for manufacturing and ISO-driven organizations.
The operational problem
Spreadsheets, paper forms and disconnected databases make it difficult to see what is happening now, who is responsible and what still needs attention.
The CIS approach
CIS turns quality records into controlled workflows, assigned actions and useful management information. Because the modules work together, inspection, audit, supplier, training and production data can support decisions across the organization.
Integrated capabilities
Start with the processes causing the most pain and expand as your needs grow. Each capability works independently while sharing information across CIS.
Manage revisions, reviews, approvals, access and complete document history.
Explore CIS document managementPlan audits, capture evidence, assign findings and follow actions through completion.
Explore the CIS auditing systemDefine requirements at the product level and capture inspection results on the shop floor.
Explore the CIS inspection systemSchedule work, prevent overdue activities and preserve complete equipment history.
Explore calibration and maintenanceConnect job control, inspection checkpoints, materials and operational visibility.
Explore production and inventoryConnect qualifications, training requirements and employee records to controlled processes.
Explore HR and training managementControl nonconformities, root cause, corrective action and improvement from detection to closure.
Explore quality and improvement toolsEvaluate suppliers, monitor performance and connect vendor records with incoming quality.
Explore vendor and supplier managementForms, fields, workflows, permissions and reports can be adapted to your organization’s requirements.
Operational outcomes
CIS is designed to make current information visible and actionable—not merely store records for the next audit.
Customer recommendations
Customers describe practical improvements in control, accessibility and the ability to adapt CIS to their operations.
Wacom Quartz reports that CIS improved calibration and maintenance scheduling and supported its move to a paperless ISO 9001:2015 quality management system.
Wilson Warehouse values organized documentation and temporary auditor access, which allows relevant information to be reviewed securely and efficiently.
Astroseal highlights the ability to customize CIS around its business needs and the customer service provided by the TQMS team.
A practical implementation path
Implementation does not need to be an all-at-once project. Many organizations begin with the processes creating the greatest risk or administrative burden, then expand CIS in manageable stages.
Focus first on the processes where delays, poor visibility or manual follow-up cause the greatest problems.
Set up users, permissions, forms and workflows, then train the people responsible for operating the selected processes.
Add connected capabilities as your team gains confidence and your organization is ready for the next improvement.
Experience behind the software
TQMS combines decades of hands-on quality-management experience with dedicated CIS development and customer support.
Quality-management insights
Learn why effective internal audits need clear objectives that go beyond confirming compliance.
Read the audit objectives articleExamine the gap between written instructions, employee understanding and demonstrated competence.
Read the Bowtie Approach articleDiscover why identifying and resolving problems is essential to meaningful continual improvement.
Read the nonconformity articleTell us where your quality system is creating delays, risk or unnecessary work. We will show you how CIS can address those priorities in a focused demonstration.