Quality Management System Software Since Year 2004

Specifically developed according to ISO Document Control requirements. Its automated workflow includes document creation, review and approval, publishing, revise, revision control, obsolete document archiving, document change record, document master list, document cross-reference, notification on pending task, etc.

Simplifies ISO Audit compliance. Enables organizations to manage entire audit process include planning, execution, approval and reporting of ISO Audit is complies with regulations and compliance requirements.

Provides company to controls the CAPA process right from creation to validation and closure. Identifies and addresses the root causes of quality issues while supporting ISO compliance, lowering risk of business impact and repeat issues, and fostering continuous improvement to achieve QMS objective.

Automates entire SCAR process end-to-end right from initiate a SCAR with critical information, investigate and determine actual root cause, perform risk assessment, identify and implement action plan, perform verification and effectiveness steps and resolve the deficiencies.

Makes it simple to keep track of calibration records and manage process in a cloud-based solution. It offers everything you need to document control, schedule and manage calibration requirement include specific calibration criteria, assign schedule, managed unscheduled or emergency calibration, calibration report and certificate, etc.

Designed to accurately identifies, capture and track all nonconformance, customer complaints, analyse, develop action plans, and use data with analytics insights to correct and prevent reoccurrence. It helps to optimize customer success, satisfaction, and retention.

Simplifies processes to initiate, monitor, measure and improve the quality objective results and performance. It helps to make the Quality Objectives effective in addressing what needs to be improved, which aligned with the S.M.A.R.T (specific, measurable, achievable, realistic and time-based) concept.

Provides systematic mechanism for organization, especially process improvement teams to assess, analyse the quality gap of current business performance to the long-term goals, identify action QMS action plan, generate comprehensive gap analysis report for improvement.

Provides systematic framework to simply the identification, analysis, monitoring, reviewal, approval, treatment, unify all risk-related activities and documents for effective, manageable and consistent risk management.