niix QIS is a comprehensive quality assurance system with eight major elements greatly improve management visibility with live and real time monitoring on variety of potential issues ranging from customer complaints, non-conformance, preventive action and prevent issue and task from going unaddressed.
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![]() Enable employees to make suggestions or comments directly into tracking system on how to improve operations or systems within the organization with a systematic pre-defined workflow. It streamlines the suggestion process, report on findings, and make changes to improve the organization and it is a more organized way of getting better.
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![]() Enable the organization to manage the procedure or work which is not conformance to the documented procedures as it supposed to be. This system will help your business increase efficiency by converging communications technologies in order to work more efficiently and thoroughly tackles any non-conformance works, products and services.
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![]() Offer a systematic way to handle the corrective action to be taken in respect to meeting compliance, identify the problem to be resolved within specific due date. Inputs to the Corrective Action Request may be directed from customer complaints, including the return of defective products, quality system non-conformances discovered during internal or external audits. The system enables tracking of assigned corrective actions to be solved in timely manner, and prevent from happening again. This will help the organization to provide any follow-up training to related employee or make changes in the operating procedures and etc.
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![]() Enable Supplier Issue Tracking such as supplied non-conforming parts or supplies, issues resulting from supplier non-conformances, delivery schedules or other related issues. SCAR can be created and assigned to specific supplier which the supplier shall access to the system and response to the specific SCAR within the assigned due date. It gives your suppliers the ability to initiate their suggestions or answer a non-conformance with documented record.
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![]() Enable the company to initiate and monitor ICAR on any defect products or non-conformance identified during internal audits. Further investigate and mitigate any impacts caused by the occurrence of non-conformance with a pre-defined systematic way. Once a corrective action had been identified, the problem shall be resolved within the given period. And take action as quickly as possible. Make sure assigned responsibilities for actions and schedules are clear so that correction occurs in a timely manner, and prevent from delivering defect products to the customers and to prevent from reoccurrence.
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![]() This module offer a systematic way to handle the internal preventive action to be taken when any possible non-conformance had been identify internally, but not yet happen. Once a preventive action had been identified, the possible problem shall be resolved within the given period where take action shall be taken as quickly as possible. Make sure assigned responsibilities for actions and schedules are clear so that correction occurs in a timely manner, and prevent from happening.
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![]() This module offer proper meeting scheduling planning in advance with specific meeting date, time, meeting agenda and participants. All the meeting minutes can be updated in the system and keep for record purpose and easier for future reference.
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![]() This module enables company to properly plan and schedule the audit time frame in planned interval and in advance. With this system, the company can identify which area to be audited, by who, when, and other details. The audit detail can then be assigned to specific individual for preparation and to take further action. The audit reports details can then be updated in the system for and keep for record purpose and easier for future reference.
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