QualityPro

Menu

How Does QMS Software Work for the Chemical and Agrochemical Industry?

Chirag Panjwani on August 25, 2022

QMS software for chemical and agrochemical industry

If you have landed up on this blog page, probably you are a chemical or agrochemical industry manufacturer looking for a tool that can help you with managing the quality of your products or services. As this industry has a lot of things to manage from quality of materials to packaging, environmental incidents to toxic dispersions, etc., you need a comprehensive quality management software for chemical industry that can align all the organizational processes, activities, and systems with compliance standards to ensure minimum environmental, health, and safety hazards involved.

Chemical or agrochemical manufacturing has under its umbrella- fuels, pesticides, paints and solvents, cleaning chemicals, disinfectants, etc., industries and managing the quality of these products while keeping safety first is not at all an easy task.

This blog will include:

  • Overview
  • Challenges chemical and agrochemical industry faces
  • Enter Next Gen eQMS for chemical & agrochemical industry
  • QualityPro’s effectiveness in managing chemical and agrochemical industry
  • Concluding Thoughts

Overview

To begin with, QMS for chemical industry is an advanced quality management tool that helps chemical and agrochemical manufacturers get better visibility and traceability into their quality processes.

This means they can manage entirely each, and every component of their processes related to quality seamlessly and effortlessly. Let’s now know the challenges this industry experiences and how QMS helps.

Challenges chemical and agrochemical industry faces –

On the path to achieving quality management, chemical and agrochemical manufacturers encounter various obstacles, such as new compliance requirements, patent registrations, re-registrations, verifying third-party suppliers, etc.

They are tasked with managing the demands of a supply chain that is becoming more intricate and global. They struggle to manage compliance with regulations like OSHA, EPA, ISO, etc. In addition to monitoring product quality and enhancing supplier-vendor relationships, they aim to launch products more quickly. Moreover, they must ensure that none of the dangerous chemical substances endanger the safety or health of their workers. These difficulties multiply in complexity when the production or packaging process is not transparent and traceable.

Therefore, a quality management system for chemical industry can have a significant positive impact on  manufacturing companies of all sizes and types, resulting in greater productivity, lower operating costs, better information flow, and improved performance management.

Enter Next Gen eQMS for chemical & agrochemical industry

A thorough QMS for chemical manufacturing industry incorporates the rest of the business in terms of the legal duties for environmental, health, and safety protection. By following SOPs, getting alerts for all deviations, and following the industry best practices, chemical industry operators can rest assured to get consistent product quality.

A Quality Management Software for chemical industry should be able to provide the following benefits, then only it is recommended the most:

Benefits of QMS software for chemical industry

QualityPro’s effectiveness in managing chemical and agrochemical industry

QualityPro offers chemical businesses with built-in quality methodologies and advanced user workflow to help companies manage and track Quality Management Systems. It elevates organizations into a collaborative and paperless environment for ongoing improvement while lowering the overall administrative costs of maintaining quality at every level, thanks to its integrated modules for quality and compliance management.

QualityPro is available as a stand-alone eQMS solution and can be integrated with BatchMaster ERP products, including BatchMaster ERP for SAP Business One. The modules are fully connected, enabling quick data transfer between them, execution of corrective actions straight from complaints or adverse events, and tracing and tracking of the data from the source to the event and back. This creates and stores an audit trail of the whole event for future use.

Being a cloud-based QMS software, it creates a sole source of truth for products, processes, and quality data, ensuring that each stage of the process is synchronized and compliant. It allows all relevant stakeholders to quickly communicate, store operational processes, and retrieve records in real-time.

This is how the software works effectively for the agricultural and chemical industries:

  • Maintains the audit trail of documents viewed, accessed, and modified by any user
  • Maintains and tracks nonconformity records and suggests preventive actions accordingly
  • Records the corrective measures taken to prevent the recurrence of non-conformance
  • Performs verification and maintains the effectiveness of CAPA or any other vital information related to the CAPA verification process
  • Stores documents in a centralized database for resolving customer complaints
  • Supports change management cycle

Concluding Thoughts

We truly hope that this blog was able to clarify how QMS software for the chemical and agricultural industries works. QualityPro, a comprehensive QMS for chemical industry brings the entire organization in agreement with the regulatory standards for safety, health, and environmental care. By following the industry best practices defined as key quality requirements, chemical industry operators can rest assured to get consistent product quality.

You can reach us at contact@bmqualitymaster.com for a free consultation.

What is Electronic Quality Management System (eQMS Software)?

Chirag Panjwani on July 27, 2022

what is electronic quality management system

Overview

Historically, paper-based and spreadsheet-centric quality systems were used to monitor and analyze quality-related data. Manual data entries and disconnected files made it difficult to track and manage quality-related information. Regarding challenges, while addressing top-quality management objectives for life sciences industry, respondent results were:

Quality management software (eQMS Software)

All thanks to the evolution of integrated IT-based systems like eQMS that made it easier to record and report quality variables across various access points. This blog discusses the definition, functions, benefits, and future of eQMS software with respect to total quality management.   

What is Electronic Quality Management System?

An Electronic Quality Management System (eQMS) is a software solution designed to electronically handle, document, and manage quality-related processes within an organization. Its primary objective is to ensure that products meet required standards, are free from defects, and operate within defined tolerances.

This software encompasses a range of techniques, structures, processes, and resources necessary for efficient Total Quality Management (TQM) practices. By leveraging an eQMS, organizations aim to enhance process efficiency and minimize human error.

One of its key advantages lies in its ability to proactively identify potential quality issues before they manifest. It grants enhanced visibility into Quality Assurance (QA) and Quality Control (QC) processes within a manufacturing organization.

Core functionalities of an eQMS include compliance management, change management, investigation of adverse events, initiating corrective and preventive actions, managing risks, and integrating complaint management into the quality process.

The system operates as a closed-loop, ensuring accountability at every level of the quality management process.

eQMS software can be implemented through various deployment models such as on-premise, cloud-based, or hybrid setups. This flexibility allows organizations to choose based on their data access requirements.

Furthermore, these systems often offer integration capabilities with other business management software such as Enterprise Resource Planning (ERP), Customer Relationship Management (CRM), Product Lifecycle Management (PLM), and Manufacturing Execution Systems (MES) to streamline operations across different departments and processes within the organization.

Difference between QMS and eQMS

The difference between a Quality Management System (QMS) and an Electronic Quality Management System (eQMS) lies primarily in their operational modes, capabilities, and efficiency in managing quality-related processes:

Operational Approach:

  • QMS: Traditionally, QMS may rely on manual processes, spreadsheets, or paper-based documentation to manage quality-related operations. These methods can work independently, potentially leading to discrepancies and various versions of information.
  • eQMS: eQMS integrates all quality management functions into a single, unified software system. It stores and manages all quality-related data in a centralized location, offering a single source of truth and reducing the risk of version discrepancies.

Data Accessibility and Security:

  • QMS: Paper-based or spreadsheet-centric QMS can limit access to updated documents and lack a comprehensive record of changes.
  • eQMS: Ensures access to updated, authorized documents, and maintains an audit trail of all changes. Unauthorized or unsigned documents are flagged, enhancing data security and compliance.

Regulatory Compliance:

  • QMS: Managing regulatory compliance can be challenging with traditional QMS, potentially leading to compliance issues due to manual processes and inadequate documentation.
  • eQMS: Provides convenience and ease in handling regulatory compliance documentation by offering features specifically designed to manage compliance requirements effectively.

Develop a Culture of Quality…

“55% of respondents who don’t own enterprise quality management software (eQMS) say their quality metrics aren’t properly measured.”- LNS Report

The effective utilization of an Enterprise Quality Management Software (eQMS) is pivotal in fostering a pervasive culture of quality within an organization. When every individual within the company embraces a quality-centric approach and resources are aligned to deliver superior products, it reinforces a culture committed to excellence.

Specifically designed to optimize various quality-related aspects in manufacturing, eQMS software ensures streamlined maintenance of factory equipment, meticulous inspection of raw materials and finished goods, and proficient handling of quality audits.

Successful eQMS implementation yields numerous benefits, including heightened product quality, reduced product recalls, minimized wastage, and fewer warranty claims, all contributing to improved operational efficiency.

eQMS systems offer robust data integration capabilities, consolidating quality-related information into a unified database. This integration drives continual improvement across the entire product life cycle.

Additionally, eQMS solutions are conveniently scalable, adapting seamlessly to the growing needs of the manufacturing organization. By eliminating departmental silos and establishing automated alerts for immediate attention to quality issues, eQMS promotes accountability.

Addressing the culture of quality, ISO 9001:2015 serves as the primary regulatory guideline, ensuring the adherence to specified quality standards across the organization.

eQMS software aligns with ISO 9001:2015 requirements, ensuring that processes, individuals, systems, resources, and final products meet the stipulated standards. This guideline outlines key characteristics for a company’s culture, emphasizing quality in business processes, workforce efforts, and the end product.

What are the Features of an Electronic Quality Management System?

Specific facets of total quality management require specific features to be included in the eQMS system. Below listed are the most important functions of eQMS:

Features of Quality Management System
  • Non-Conformance – It is important to identify product issues by testing for quality and eQMS helps the organization identify events of non-conformance in following the SOPs. Valid issues are considered for further actions, while invalid issues are terminated on the spot. eQMS also records all the actions taken to correct the non-conformity.
  • CAPA – When a non-conformance issue is identified and found to be valid, eQMS initiates the process of improvement. It specifies the corrective actions that need to be taken in terms of change in process and the preventive action required to rework/scrap the product, so that the final product quality is maintained up to the standards.
  • Complaint Management – The eQMS software helps manufacturing organizations establish a complaint handling process. The entire complaint management life cycle from documenting the problem, performing root cause analysis, providing timely response to the customer, and triggering internal CAPA is integrated into the eQMS system.
  • Change Management – When a process change is required or a CAPA issue is raised, the eQMS system manages and documents the entire change control process. It helps businesses automate the entire change management process starting from initiating change requests, impact evaluation, actual implementation, and culminating with verification and closure.
  • Training Management – eQMS helps organizations keep their employees updated with the latest certifications on all controlled documents in the organization. It helps manager identify training needs and keeps track of employee performance throughout the process. The eQMS software can also issue certificates on completion of the training modules.
  • Document Management – eQMS manages all the critical documents of the organization from creation to approval & publishing to archival. Along with updating to the latest version of the documents, eQMS also facilitates the removal of obsolete files. It can also create a master list and document map to track document changes.
  • Compliance Management – eQMS can help manufacturers by maintaining a clear list of compliance requirements. It automates the tracking and control of compliance-related activities like documentation, planning, reporting, audit, etc. eQMS also simplifies the reporting of non-compliance events to save the company from legislative action.
  • Risk Management – eQMS takes a very structured approach to identify, assess, control, communicate and review all the quality risks in the organization. With eQMS, organizations can take actions to ensure that any anticipated problems don’t occur and if they do, have a control mechanism to rectify them.
  • Audit Management – eQMS helps organizations conduct internal and external audits to enhance product quality. It can schedule, structure, perform and assess periodic and ad-hoc audits within the specified time frame. The audit management functionality also helps organizations meet industry-specific compliance requirements.

What are the Benefits of Electronic Quality Management Software?

An eQMS can transform the manufacturing organization in terms of men, machines, materials and methods. Below are the major benefits of an eQMS:

  1. Enhanced Effectiveness: Clearly defining and achieving quality objectives set by the organization.
  2. Cultivating a Quality Culture: Instilling a values-based system focused on maintaining high-quality standards across the organization.
  3. Streamlined Data Management: Establishing a centralized database for consistent and accurate data management, ensuring a single source of truth.
  4. Enhanced Accessibility: Enabling access to the system from multiple devices such as laptops, smartphones, and tablets.
  5. Improved Audit Functionality: Setting tolerance levels and creating audit trails to facilitate effective audit processes.
  6. Increased Customer Satisfaction: Adhering to quality policies and implementing streamlined processes directly impacts customer satisfaction.
  7. Enhanced Compliance: Maintaining updated compliance records and automating alerts to ensure adherence to regulations.
  8. Improved Documentation: Defining and documenting critical processes and objectives systematically for better clarity and understanding.

Final thoughts

eQMS focuses on the consistency of the process. It ensures that every time a production cycle is performed, the same information, material, methods, skills & controls are applied in a constant manner. Along with heightened productivity, an electronic qms software helps prevent costly mistakes, enhance product management, improve risk forecasting and establish quality metrics. Therefore, it is important for organizations to implement an eQMS and QualityPro can prove to be a perfect choice.

Get QualityPro today and enjoy the benefits of end-to-end quality management. Feel free to write to us at contact@bmqualitymaster.com, or contact us to know more about it as well as our other products.

Things to Consider when Implementing a QMS System

Chirag Panjwani on June 3, 2022

QMS implementation

Manufacturing companies use Quality Management Systems to identify faults in their processes and fix them by optimizing and standardizing them. This blog will guide you in comprehending the concept of quality management as well as the important things to consider for the implementation of QMS system.

Table of Contents:

  • Overview
  • Defining Quality Management System
  • Result of a successful QMS implementation
  • Things to consider when implementing a QMS System
  • Summarizing thoughts

Overview

Businesses all around the globe are mounting their confidence in QMS systems to produce high-end quality products.  They have recognized the need for an inclusive QMS software and are deploying it with the objective of enhancing the quality of their business processes, staying compliant with the stringent rules, and satisfying the customer demands. They, these days, are proactively assessing and investing in QMS solutions to ensure that quality standards are maintained at every stage of the product lifecycle.

Defining Quality Management System –

Before diving into the subject, here’ a quick brush-up on what a QMS essentially is-

Quality Management System (QMS) is a system that documents processes, procedures, and responsibilities for achieving quality policies and objectives. A QMS helps coordinate and direct an organization’s quality-related  activities to meet customer and regulatory requirements and improve its effectiveness and efficiency on a continuous basis. Quality control systems are used by businesses to assess the quality of all factors involved in manufacturing and to ensure that the products or services meet their technical standards.

The implementation of a QMS system results in process improvement and standardization, as well as ensuring product and service quality.

QMS overview

Why a QMS implementation?

  • Achieves organizational goals.
  • Reduces costly errors.
  • Improves customer satisfaction.
  • Improves documentation.
  • Identifies issues and rectifies them.
  • Creates a culture of quality.
  • Better internal communications.
  • Consistent products quality.
  • Improves compliance.

Things to consider when implementing a QMS System –

Implementing a quality management system is not child’s play. It requires a huge amount of effort to put in. Companies need to take inputs from their staff members at all levels, right from the top management (the decision-maker) to the lower management. Once everyone gets on the same page, the aforementioned step should be followed for a QMS Implementation in manufacturing:

Need Analysis:  A thorough analysis or an internal audit should be conducted. Companies should gather all the key business requirements and determine the software’s true need. They should calculate the anticipated risks and break down the important areas that will give significant consumer satisfaction. It will give businesses a good understanding of where the current procedures are lagging and what the new system will do.

Planning: Make a list of the gaps in the current processes based on the analysis of the quality management processes. It will enable companies to go on to the next step of gathering resources and establishing an effective implementation strategy. Divide the project into sub projects and assign a deadline for each. Put up a team that monitors if the implementation progress takes place in the specified time frames or not. Any delays should be brought to the notice of top management and should be accounted for.

Bringing team & stakeholders on the same page: Ensure that all the employees from the top to the bottom are involved in the project. They should know about the new system. Furthermore, all stakeholders should be trained on using the new system.

Teamwork: Form a team to deal with the issues related to the software. It should be composed of people from several departments, with someone in charge, ideally from the quality or IT departments.

Selecting the system: Select the appropriate solution after articulating the needs, and search for key business-critical variables. Know about frequent updates, vendor support in terms of training and maintenance, etc.

Deployment phase: Deploy the system and validate that it is compatible with all existing business systems and that it has been configured to meet specific needs. Collecting and migrating existing data to the software’s database is also done at this stage.

Control & Measure: Set some benchmarks for evaluating the new system’s performance. Define the procedures for controlling, measuring, and monitoring outputs to verify that they satisfy quality standards.

Review process for continuous improvement: Schedule product or process audits to ensure that policies and requirements are met. Companies should continue to audit and assess the procedures on a regular basis to ensure that they are evolving.

Summarizing thoughts:

By following the steps mentioned above, businesses can implement an effective QMS system. Contact us to know about an expert partner who can assist you with the implementation of quality management system in manufacturing. Our in-house quality experts at QualityPro will be pleased to help you.

What is Document Management System (DMS)?

Chirag Panjwani on June 1, 2022

Document Management System

Do you know what all companies have in common? It doesn’t matter if it’s the IT industry, healthcare, manufacturing, automobiles, cosmetics, finance, or any other industry, they all rely heavily on documentation.

Documents are the foundation of any company. Documents play a critical part in the smooth operations and ultimate success of it.

There isn’t a single business on the planet that can get through a day without reading and sharing papers. This comprises of, among other things, marketing brochures, project proposals, technical documentation, training materials, etc.

Yep. Documents in the workplace are essential!

The difficulty is that the more documents we create and rely on for work, the more important it is to have processes in place to manage them across the organization. And, a Document Management System can be a best bet for this.

But, first thing first-

What is actually a Document Management System or DMS?

As the name implies, a Document Management System (DMS) is a system or software that makes it easier to create, store, manage, index, protect, and retrieve digital documents. Although the majority of Document Management Solutions store all of your digital documents on the cloud, they are much more. In a true sense, it is a framework that allows vital information to flow freely throughout a company.

A competent Document Management System may help you organize all of your files and data in one place, maintain track of all of your key papers, increase accuracy, and enable 24/7 access to documents from anywhere in the globe. As a result, using it allows you to stay ahead of the competition by providing all of the information your staff requires to complete their tasks effectively.

What’s more? Document Management System is totally off the charts!

Apart from helping make all of the tasks associated with document management easier, faster, and more efficient, DMS offers numerous reasons why a company should use it right away. Here are a few examples:

1. Reduced Storage Space

Any business can benefit from a software-based DMS that eliminates the need for file cabinets, boxes, and storage bins, freeing up valuable office space.

2. Enhanced Security

To protect sensitive data, document security is crucial for enterprises of all sizes. Access to sensitive information can be regulated at the folder level for different groups or individuals. In addition, a DMS keeps a track of who has viewed a document, when it was accessed, and how it was altered. Documents that are managed are highly traceable and can be labelled to trigger automated alerts.

3. Improved Regulatory Compliance

Meeting certain compliance standards manually in document management can be rather complicated. At the same time, non-compliance can result in fines, license suspension, and, in some situations, criminal liability. Sarbanes Oxley and HIPAA, for example, are federal and state regulations that require tight security and privacy guidelines. However, non-compliance is less likely with a Document Management Solutions.

4. Easier Document Retrieval

Finding and recovering papers can take a long time, and we all know that is ultimately taking money out of our pockets. The average office worker spends 30 to 40% [Source: Forbes] of their day looking for printed documents, while businesses spend $20 on labor to file a document, $120 on labor to find a misfiled document, and $220 on labor to reproduce a lost document [Source: Konica Minolta]. These excessive document management expenditures chew into a company’s budget, hinder productivity, and limit its potential for growth.

A Document Management System can be a time-saving and powerful tool. A DMS can retrieve files based on a word or phrase in a document, depending on the solution used.  It also allows users to access documents from afar. Documents can be accessed from anywhere at any time as long as there is an internet connection.

5. Better Collaboration

Acting as a central repository, an advanced Document Management System Software substantially simplifies the ability to access documents and collaborate. It gives more visibility into business processes and allows for improved workflow monitoring. 

6. Better Disaster Recovery and Backup

A data backup and disaster recovery plan are included in a well-designed Document Management Solution. Documents are protected from fire, flood, and other disasters with digital archiving as a back-up. Documents are also easily traceable and may be tracked using a variety of criteria using a DMS. Thus, it lessens the possibility of papers being misfiled or lost after they have been seen.

7. Productivity Improvements

With all the data and documents just a click away, the team can put all its efforts in just working rendering higher productivity, every single day. Staff morale and client satisfaction can both benefit from faster and more efficient document retrieval.

So, what are you waiting for? Turn over a new leaf with QualityPro’s DMS and stop putting your files into a closet no less than a well.

QualityPro’s Enterprise Document Management System is a feature-rich desktop and DMS that allows you to save, create, track, retrieve, and manage all types of documents. It supports the complete document lifecycle for an organization, from content generation through distribution to archiving and, finally, secure content retention and deletion.

In a nutshell, it unifies your document management requirements into a single, cost-effective system. Furthermore, it is simple to use, has a simple interface, and provides a high level of flexibility, allowing businesses of all types and sizes to use it to suit their document management needs.

As a result,  Cloud-based Document Management System is getting popular in businesses that want to become paperless. Want to be in same boat? If yes, ask for a demo now!

Benefits of a Functioning Nonconformance Management System

Chirag Panjwani on May 5, 2022

non conformance management

“You are into a business of manufacturing glass studs of size 50 mm. But an inspection revealed that a particular lot of the studs measures 45 mm.”

“A product you recently delivered to a customer didn’t match their specification, and was of a different color. More so, it was delivered to a wrong address initially. You came to know this when a customer complaint was received in this regard.”

“Crucial details such as temperature information, and the supervisor’s signature, are missing from your batch records.”

“A reduction of quality at your plant floor has been experienced due to a certain manufacturing procedure.”

What do you make of these statements?

These are all examples of nonconformance, or nonconformity, which essentially means that something has went wrong somewhere; either in a product, a service, a process, material from a supplier, or in the management system itself. It basically is an activity or a process which doesn’t fulfil its intended purpose.

A nonconformance in quality management generally occurs when something some way does not meet the specifications or requirements that could be defined either by a customer, or a regulatory body, or by an organization. It is ubiquitous, can happen anywhere, and at any time in a business, and is usually identified externally by customers, or auditors, and internally by testers or staff from other departments.

Any nonconformity or nonconformance in quality management can result in bad customer experiences, rework, product recall, and may even impact the organizations in terms of cost, reputation, productivity, and efficiency. It is important for the businesses to identify and address them in a timely manner through corrective actions and preventive actions (CAPA).

Non-Conformance In Terms of ISO

The international standard that highlights the requirements for a quality management system (QMS), ISO 9001 ensures that a business organization consistently offers quality products and operates appropriately under its regulatory measures. And if it doesn’t operate up to the set standards, it’s called non-conformance.

ISO 9001 defines nonconformance in quality management as the failure to meet one or more of the existing requirements. When an organization goes outside the regulatory boundaries, it must control and fix the problem before continuing business. Failure to do so may lead to the company’s downfall, as these standards mean everyone needs to play by the same rules.

Satisfying their customer base is one of the biggest objectives of organizations, and the ISO 9001 standards have been put in place to ensure that this objective is met, along with the other objectives such as quality and safety for the employees as well as the customers, high employee morale, etc. If not for these standards, the organizations wouldn’t be held responsible for their business practices and actions.

Nonconformance Management System- The Secret to Efficiently Managing Non-conformances

No wonder, managing the nonconformances is of great significance for business organizations; especially the ones that put great value on quality of their products, services, and processes. For all such organizations, nonconformance management is a very handy quality tool which can quickly determine systemic issues within the business.

Nonconformance management is fundamentally the process whereby the business organizations manage nonconformances in a way that they are promptly identified, properly documented, thoroughly investigated, and appropriately segregated and dispositioned on the basis of applicable regulations and standards.

And for effective as well as efficient nonconformance management, organizations rely on a nonconformance management software. The investment made in a nonconformance management system is a massive decision, and can potentially make or break an organization. That’s why the businesses need to invest in the right software, which can offer a number of benefits.

Here’s What a Functioning Nonconformance Management System Can Offer

Nonconformance in quality management requires a robust tool that provides features and support to identify and manage product conformance. The features mentioned here include the steps required to recognize and resolve the nonconformance issues from all sources, including identification, remedial action, root cause determination, CAPA, etc.

A functioning nonconformance management system allows users to:

  • Identify and register any nonconforming materials, and keep a track of them.
  • Set processes, due dates, escalations, and even notifications to ensure the materials are managed quickly and in a timely way.
  • Link deviations to any nonconformance records, and initiate corrective actions.
  • Create a history of risk within a product, process, supplier, or production line.
  • Close the loop on nonconformances by initiating change management, so that improvements can be made organization-wide, and risk of recurrence could be mitigated.

Investing in the right nonconformance management system has immense benefits for the businesses. Check out the benefits of an effective, and functioning nonconformance management software:

  • It helps businesses streamline their conformance processes
  • It allows businesses Identify any materials that don’t conform, and also the areas that require action
  • It helps avoid the risks of escalated nonconformance costs, including the internal/external failure costs, regulatory fines, etc., and also in terms of reputation and resources
  • It improves quality processes by facilitating efficient use of resources
  • It allows businesses to easily see where their procedures aren’t working as planned, thus giving them an opportunity to address this and improve the effectiveness of their system
  • It provides the businesses with an opportunity to drive continual improvement by consistently addressing their nonconformity.
  • It brings down the quality costs substantially
  • It facilitates stronger collaboration and a better risk response

To sum up

Nonconformances, as we mentioned above, are ubiquitous. In addition, they are inevitable, and can adversely affect the businesses in more ways than one. It is essential for businesses to identify and address them in the most effective as well as timely manner. For the same, they turn to a nonconformance management software.

A functioning nonconformance management system could be a standalone solution, or a part of a QMS software. Regardless of how it comes into the system, it should address risks and allow the internal/external stakeholders to browse reminders, conformance notifications, and the escalated issues related to quality.

It makes sense for businesses to invest in a fit-for-purpose nonconformance management system that delivers these benefits. If your existing system is not good enough, it would be prudent to explore other options such as QualityPro, a best-in-class QMS with a potent nonconformance management functionality, to quickly see these benefits. Write to us for more information, or to schedule a demo.