Non conformance Management

In simple terms, a NonConformance refers to the occurrence of a problem that needs to be immediately addressed. The issue/problem is reported as a nonconformance only when a product(s) does not match the specifications or requirements set by the companies’ quality standards.

Amzur’s Nonconformance Management software (QNC) is designed to
complement your existing nonconformance process streamline your organization tasks in

  • Identify the Issue
  • Document/Report the Issue
  • Evaluate/Review the Issue
  • Segregate the NonConforming Material
  • Disposition of the NonConforming Material
  • Investigate the NonConforming Material for CAPA

Amzur’s Nonconformance Management Software system is enabled with powerful analytics and reporting capabilities that enable you to access critical defect information to make informed quality decisions.

A nonconformance issue arises when a product does not meet the specifications or requirements as required by your compliance targets/goals. Such issues need to be identified, documented, and resolved on an immediate basis, based on compliance and quality standard targets.

With Amzur’s  Nonconformance Management system, you can address such issues with a simple initiation and product information gathering step. The initiation step allows you to capture key information about the product such as:

  • Defect Statement and Code
  • Occurrence Date
  • Reported Date
  • Reported By
  • Location
  • Products and Lot/Batch number and Quantity
  • NC Owner and others

Additionally, you can customize the new fields based on your business structure to capture the requisite information. Once you have completed the record creation, you will get a unique system generated reference number to track the remaining processes.

Once the issue has been identified and recorded, the next step calls for the evaluation and review of the issue to determine the investigation progress regarding the nonconforming material(s).

Exactly what do the Amzur’s nonconformance resolution steps allow you to do? This step gives the NC owner the option to utilize a Risk Assessment for a thorough review and identification of the next steps in the process. If you find that the issue reported is not a valid nonconformance after evaluation and review, you can simply close the record stating the reason. However, you could continue with the NC process by creating a new CAPA or link it to an existing CAPA issue that has been previously identified as a valid nonconformance.

We understand that every nonconformance requires a different level of an investigation depending upon the material-type, component(s) and product(s) involved along with the complexity, suspected or confirmed impact on the product’s performance or intended use.

The Amzur’s Nonconformance Management system software comes with a user-friendly, intuitive interface that allows you to select/de-select the tasks, define task owners and due dates that are necessary for each nonconformance record.

The nonconforming material must be identified and segregated in a controlled (Containment) area to prevent being used inadvertently until the material review board (MRB) makes a final disposition.

With Amzur’s EQMS software, you can identify and document the material under this product information step along with relevant details such as batch, lot or serial number, and the quantity associated with the nonconformance. Further, you can use the containment task to specify the actions taken for the segregation of the nonconforming material.

You can also integrate Amzur’s Nonconformance management system with your existing ERP solution to signal to place a ‘Quality Hold’ on the lot, batch or serial numbers of the suspected materials for proper segregation and containment.

After the identification, tagging, and segregation of the non-conforming material in a controlled area, the MRB or authorized expert can make the final disposition call. A written rationale or justification for disposition decisions needs to be documented with an electronic signature for the approving regulatory authorities.

In Amzur’s nonconformance management and reporting software module, you can use the disposition task to document the final disposition and all its relevant information. It comes with a built-in mistake proofing technique that tracks and alerts you about the completion of the disposition activities. It also keeps you notified in the case when the identified non-conforming material has not been completely dispositioned.

The investigation of a nonconformance is one of the most important steps of the quality management system. It must be reported and properly documented.

Qualityze NonConformance management and reporting system enables you to combine the Investigation and Implementation tasks together to allow the effective documentation of nonconforming material. In the Investigation task, you also need to document the root cause. Our NonConformance solution allows you to list multiple root causes and defects associated with the NonConformance. And finally, in the Implementation task you need to define the action plans to correct the root cause with corrective, preventative action plan.

Amzur NonConformance Management Software for Multiple Industries

Amzur NonConformance Management System works for many industries with the same effectiveness and efficiency. From nonconformance management software for life sciences to Complex or General Manufacturing, Automotive, Aerospace, Healthcare, biotechnology, Pharmaceuticals, Logistics, Medical Devices, Food and Beverage operations, ours is a solution that makes it easy for you to maintain high quality standards with:

Configurable Cloud-Based Platform

The Amzur nonconformance management system is built on the world’s leading a cloud-based platform Salesforce.com. Allowing you to easily configure it to your individual requirements. It is a flexible and scalable solution that expands as you grow. If you are in the automotive industry, you can simply opt nonconformance management software for the automotive industry to manage your quality processes.

Adherence to Compliance Standards

For every industry, Amzur follow the relevant standards requirements set by the regulatory committees such as Food and Drug Administration (FDA) – 21 CFR Part 820, International Organization for Standardization (ISO) – ISO 9001, ISO 13485, Pharmaceuticals and Medical Devices Agency (PMDA), Therapeutic Goods Administration (TGA), China Food and Drug Administration (CFDA), etc.

User-Friendly Interface

Amzur nonconformance management and reporting software are built with an intuitive interface so that any user can operate it with utmost ease by simply entering the field data correctly. The need for technical expertise is eliminated especially for industries like General Manufacturing. You can use the nonconformance management software system in Manufacturing with complete ease.

Why NonConformance is Important?

The recording of Nonconformances is an important step in keeping high-quality standards while identifying opportunities for continuous improvement. It encourages any organization to:

  • Learn from its mistakes.
  • Extend their product lifecycles
  • Boost market share
  • Deliver quality products to customers

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