Alternatives to QST

Intelex delivers a unified software system for overseeing Environmental, Health, Safety, and Quality (EHSQ) initiatives. Its expandable platform is crafted to consolidate, oversee, and scrutinize EHS and Quality data comprehensively. The solution works on any device to meet the realities of your workplace. With Intelex, your organization can: Elevate your EHSQ program outcomes by supervising workflows for superior performance and command. Discern patterns and propensities through goal-setting to deepen understanding and improve decision-making in your EHSQ program. Diminish occurrences and cut down on administrative tasks by efficiently supervising, managing, refining, and extracting insights from your safety data via our intuitive safety software. Simplify the management and reporting of air, water, and waste emissions, and oversee environmental outputs to fulfill sustainability objectives. Foster ongoing improvements in quality by seamlessly logging and monitoring all instances of nonconformity within a unified, web-based system. Investigate trends across various departments, sites, or locations. Intelex can help you manage compliance with international standards and regulations such as: OSHA, WCB, ISO 45001, EPA, ISO

It is difficult to make data available and actionable when a manufacturing site has many processes. As operations grow, it is becoming more difficult to comply with safety, quality, and environmental regulations. Manufacturing is built on predictability and reliability. Manufacturing by nature is all in the execution of established processes. TenForce was built from the feedback of our clients to map the operational reality in a plant.

Intellect's QMS software has been proven to improve quality operations and reduce overall quality cost by up to 40%. Our apps were designed by certified quality professionals and can be easily customized with our no-code platform or drag-and-drop technology. Remote access for your team, mobile apps, dynamic workflows, analytics, reporting, and remote access are all possible with this modern and simple solution. Apps include Document Control and Employee Training, Audit Management CAPA, Nonconformance, as well as other useful features.

BPAQuality365, a QMS software, can be used in your secure Microsoft 365 cloud. It leverages tools used daily by collaborators and does not require you to change your user habits. It is modern, compatible with all devices, adaptable to your specific needs, and powered through innovative M365 technologies. The app includes powerful compliance document management, audit, non-conformance, CAPA action, process and process maps, incident, change, risk, FMEA, SWOT, equipment, health, safety, environment modules compliant with ISO 9001, FDA Part 11 and medical regulations. The QMS app integrates with Teams discussions and users can ask the QMS while chatting in Teams and share QMS card with their colleagues. You can go further to achieve your Quality 4.0 goals by combining powerful AI features with best-in-class workflow automation and business intelligence. BPA's Microsoft Preferred status allows you to customize your QMS to meet your needs, share knowledge with your power users, and learn about M365 technologies.

QSE SMART is an application for quality, safety and environmental management that was specifically designed for small to medium-sized businesses and projects with 5 to 500 users. QSE SMART is a solid framework that complies to key requirements of ISO9001 and 45001 and simplifies the daily running of your integrated QSE management software. QSE SMART makes ISO practical for your business. QSE SMART is based on a risk-based approach to ISO 31000. It helps you to identify and exploit key information and metrics that support your business goals in regard to quality, safety and environmental management. This includes your objectives and targets as well as management reviews, risk and opportunities, audits, inspections, management reviews, management reviews, risk and improvement, audits, inspections, audits and inspections.

Virje complies to 21 CFR Part 11, 21 CFR Section 820, ISO 13485. Are you overwhelmed by the idea of Part 11 software validation Accessible wherever you are, whenever you work. Automated collaboration and automation can help you reduce paper, lower costs, and increase efficiency. This is the ideal solution for small- to medium-sized businesses. This system was designed specifically for quality control of medical devices. The system is flexible enough that it can adapt to your workflows without having to compromise. Modifiable change order approvals can be configured by employee role or by document type. Notifications to the responsible personnel at each stage of the change process. Ability to identify material dispositions for individual documents. Access to historical and released versions of documents is easy. Quick access to document history. Tracking of locations and distribution of hard copies. Notification of periodic document review.

The eInfotree™, Quality Management System, provides a unified approach for Enterprise Information Management. It links data and business processes in a highly intuitive way. This connectivity creates a highly productive and easy workspace that facilitates organizational synergy, operational efficiency, and profitability. We offer solutions from the plant floor up to the top floor, with an integrated enterprise data and document management solution. This creates an agile business environment. eInfotree allows your organization to capture, process, and manage information more efficiently. This improves customer service, reduces costs, and provides a great return on investment. A number of modules add value to the browser-based application.

Document Control is a document management system that supports controlled processes and practices in creating, reviewing, correcting and issuing documents. The QMS QISS is an ISO-based QMS QISS Software System that automates corrective action processes in regulatory environments. Your own risk-based thinking. To reduce and mitigate your risk, centralize. Standardized workflows allow you to keep track of all changes within your organization. You will enjoy many additional benefits from a paperless document management system. Establish a culture of continuous improvement and make sure that each non-conformance is visible.

TIPQA is a tool that companies use to make continuous and measurable improvements in customer service, productivity, profitability, and customer service. Our QMS software allows industry leaders and managers to monitor compliance and manage quality throughout their supply chains. TIPQA QMS Software will support best practices in quality management and help you create a comprehensive continuous improvement plan for your company. Numerous companies who require high-quality products and strict quality control have found success with the TIPQA quality management software. TIP Technologies is more experienced in complex business processes within regulated manufacturing environments than any other solution provider. TIPQA's quality management solution allows users to be flexible, adapting to changing markets and quality demands. TIP Technologies is constantly improving its quality management system.

InstantGMP™, which replaces multiple software and/or paper-based solutions for managing your manufacturing and compliance needs, could be the key to unlocking your business's full potential. With a single, affordable software solution, you can easily increase production uptime, improve batch quality, and meet all FDA compliance requirements. InstantGMP™, which can be used individually or together depending on your business needs, delivers comprehensive, integrated software solutions that ensure quality, consistency, and GMP compliance. We will help you choose the right solution for your business today and tomorrow. You can organize, manage, and document batches electronically while promoting good manufacturing practices. Inventory Management Software that meets Part 11 requirements and GMP requirements. A complete quality system with templates, SOPs and guided workflows that is ideal for virtual biotech.

It is possible to get a complete overview of the document management system by separating all versions of a document into different modules based on their state (draft approved, valid, historic, and valid). Visual Quality registration forms are easy to create (using the built in HTML editor), and registration fields and workflows are more feature-rich than what our competitors offer. Visual Quality Web Access handles all registrations (requests, approvals, and rejections). Visual Quality is rapidly evolving thanks to the incredible Visual Quality community that helps shape the product. We are committed to providing you with the best software to build and maintain your quality management system.

iDoc is a document management system that is efficient. Automates and controls the documentation process, including distribution, organization policies and standard operating procedures. It is robust and secure in managing document management systems. It also provides real-time visibility. It streamlines all processes, including creation, review, approval, archival, and archival, and supports multiple files in controlled ways. Integration with training management system to assign training and to remove incorrect documents. This ensures accuracy for end-users and tracks compliance. Automated documentation, document retrieval with search/indexing capability, and document archive. You can easily set up labels, descriptions, and tags to help you organize information and keep track of documents. Keeps track of all documents and tracks any changes. This provides an audit trail that reports on documents and data fields.

IMSXpress is a cutting edge document control and quality management software (QMS) solution. IMSXpress Quality Management is easy to use and intuitive. It improves business efficiency while maintaining compliance. The solution offers a plethora of modules, such as document distribution, document control, internal audit, training, management review, Corrective/Preventive Action (CAPA), customer companies, risk management, preventative maintenance, measuring equipment, supplier control, and more.

Modify fields to reflect the realities of your company. Give permissions and set deadlines. Take control of Documents. Evaluate your suppliers. Create a SWOT Matrix. Create Corrective Action Status reports. All the other requirements of the ISO Standard. You will be notified by email or on the panel of due deadlines and notifications whenever you are assigned a task. For better follow-up, record comments and versions. Includes history of changes. It preserves the history of creation, edition, and derivation of collaboration processes. Planning, monitoring, and registration of processes, audits, and procedures. Attach documentation and evidence. Optimizing time, cost reduction, visualization, interaction and interactivity of processes, methods for follow-up, timely resolutions of problems. These are just a few of the many benefits of digitizing your management systems with inblue QMS.

Revolutionize your Life Sciences processes. You can dramatically improve the quality, control, and efficiency of your products and processes. Our fully compliant platform is pre-validated according GAMP5. This ensures inspection readiness at all time. You have complete control over all documents and processes. You can also customize workflows and automate when possible. You can enjoy uninterrupted workflows and full traceability with seamlessly connected and integrated modules. Our dedicated team is available to answer any questions you may have. Only the best Scilife experience is possible! Our Scilife platform automates, automates and organizes all processes in your industry space, no matter if you're in Medical Devices or Pharma & Biotech or ATMP. Click below to see which Scilife modules are available for your industry's unique lifecycle stages.

Since the early 1990's, Q5 has been working tirelessly and meticulously alongside our customers to develop best-practice, enterprise-level quality and security, safety and health audit software to ensure compliance. Q5AIMS safety, security, and quality audit software streamlines management processes to help you better manage the ever-changing business environment. Q5 Systems' "no compromise" approach is what makes us unique and why industry leaders trust Q5 Systems safety, security, and quality audit software. Q5AIMS safety audit software puts you in complete control. You can create standards, design inspections and audits, collect and interpret data, manage corrective action, and ensure compliance. Q5AIMS – Because there is no compromise when it comes to selecting quality, environmental, safety, and health audit software.

Pro-Sapien is the EHS Software on Microsoft 365. Designed for enterprises with 1,000+ employees, Pro-Sapien makes EHS easier for everyone across the company. Configurable modules for Incident Management, Audits, Inspections, Risk Assessment, Permit to Work and more make Pro-Sapien the ideal one-stop-shop for EHS management in Microsoft 365 enterprises. Mobile-responsive forms help employees stay productive on-the-go, combined with Teams integration for the ultimate easy access. Digitize your EHS forms, automate workflow, and get EHS insights in Power BI to improve performance - all on the platform you already know and love. See why Pro-Sapien is right for your organization by viewing a short demo video today.

Flexible workflow platform that simplifies your business processes The BizzMine workflow platform has been designed to be user-friendly and easy to set up. A company must have scalable, flexible, transparent, and effective business processes. A workflow management system can improve your organization's efficiency and enhance your operational operations. BizzMine's workflow application will elevate your business processes. Drag and drop makes it easy to configure processes. Get started today on your journey to Collect Collaborate and Share. BizzMine bridges between the user's business processes and the user. BizzMine's "zero-code" concept allows you to set up and maintain your business processes without the need for programmers or consultants. You can create unlimited solutions in a matter of hours or days, and save time and money.

It is quality or nothing for life sciences manufacturers. A robust system is required to ensure a smooth quality process that allows for quick business decisions and regulatory compliance. Assure-IQ is built to deliver. Combining Assure-IQ with Caliber's Document Management, Training and Learning Management systems can provide an unparalleled quality experience for organizations. Assure-IQ streamlines the entire quality assurance process. You can choose from over 30 modules to create a platform that fits your needs. To manage the entire product lifecycle, quality processes can be integrated with document management and training management. Both the on-cloud and the on-premise solutions use the most current technology to meet the changing needs in the industry. Flexible QMS integration with your company's systems can help set your own quality benchmarks.

HSI is the most trusted platform for environmental health and safety (EHS) in the workplace. EHS is a collection of safety applications that manage core daily responsibilities within your organization. It improves command, increases safety engagement, and streamlines productivity. HSI is a flexible solution that can be used by all industries and businesses of any size. Our combination of technology and content solutions helps Safety, HR, and Operations leaders train and develop workers, keep them safe, and meet regulatory and operational requirements. HSI connects your system to workers in the field and to the boardroom. It makes it easy to quickly access, enter and submit EHS data in real time.

Quality Link 7 is a combination of people and technology. It builds on our proven platform to help organizations automate processes, save time, and comply with regulatory requirements. Quality Link's document management system improves efficiency and eliminates the need for manual paperwork. This module will store and manage every document you create. This module allows you to print "uncontrolled" copies and perform other document-related tasks. You'll see a reduction in clerical tasks for quality staff by up to 90% with the improved organization. Our software converts existing documents from your previous management system and requires no learning curve. You won't have to lose your favorite applications as they can be easily integrated. Quality Link makes manual document maintenance obsolete and eliminates the need for constant monitoring.

The AssurX platform is a powerful software platform for enterprise quality management (EQMS) and regulatory compliance to reliably communicate and coordinate information, documentation, and activities. AssurX allows regulated businesses to quickly identify and control quality issues and risk exposure to avoid quality or noncompliance problems while improving workflow. AssurX QMS software is uniquely configurable to fit any established or dynamic business requirements. The system creates an electronic workflow of tasks, alerts, escalations, and approvals that can be automated to the desired level, mapping precisely to real-world operations. No other system is easier to deploy, configure, and modify. AssurX solutions integrate seamlessly to create a connected quality system. Solutions include audit management, corrective actions, training management, compliant management, document management, change control, risk management, EHS incident management, and more.

ThirdBase, a process improvement software and service company, was established in 2011 to help organizations improve their business performance. Our consultants are practical, reliable and experienced process improvement specialists who can work effectively with clients to achieve the desired results. We have experience in a variety of industries and have worked across many industries, including Banking and Finance and Insurance, Utilities and Human Relations, Manufacturing and Supply Chain, Information Technology and Consumer Products, Media, Transportation and Storage. Labour Associations, Leasing and Not-For-Profit, and Telecommunications. Clearly documented processes that are easy for staff to understand and access. The staff knowledge was used to address problems and improve opportunities.

Plex Quality Management System helps discrete and process manufacturers comply with strict industry and customer requirements. It is a closed-loop digital record system. Ensure predictable, repeatable quality delivery Clear reporting and in-line quality are key to ensuring high quality. With digital quality documentation, the enterprise can meet industry standards and comply with customer regulations. Increase repeat and new business growth through on-time delivery, better supplier management, and customer satisfaction. Quality management is an integral part of your workflows and processes. This reduces quality loss and the risk of recalls or warranty issues. It also improves your brand reputation and customer relations. Plex makes it easy to share quality requirements and documentation in real time across the enterprise. Plex allows you to create process control plans that include detailed inspection instructions and digital checklists.

Small to medium-sized businesses (SMEs) will love the cloud-based Quality Management System software (QMS). TRACKMEDIUM, a monthly subscription service, includes modules such as Audit Management, CAPA and Document Control, Management of Change (NCM), Training Management, and Management of Nonconformance Management. TRACKMEDIUM allows companies to create safer products, increase efficiency, and comply with industry standards such as ISO 9001, 14001, and OSHA while lowering costs. The Audit Management software by TRACKMEDIUM streamlines audit-related tasks. This includes creating standard audit and checklist templates and generating audit plans. It also allows for the generation of audit recommendations and tracking CAPAs through closure.

The SBS Quality Database is a simple, inexpensive, ISO 9001 compliant software program that allows small businesses to efficiency manage the Quality Management System or QMS. The database tracks corrective actions, preventive actions (CAPA), internal audits, safety improvement, supplier corrective actions, continual improvement projects. Compile and analyze Customer Survey results. Identify and minimized risk using the risk management module (FMEA & SWOT analysis) . Document QMS review meetings and results. Document interested parties as part of the Context of the organization. Use the dashboard for a quick view of the overall performance. Cloud based or locally installed options are available. The program is ideal for small businesses striving for ISO 9001:2015, API Q1, AS9100, or TS16949 compliance. Free demo downloads are available from our website so you may try before your buy.

Integrate your Quality, Health, Safety & Environmental Management Systems in the Cloud or on a Mobile Application. Mango is used by many organizations. Our clients are located in the United Kingdom, Australia and New Zealand, as well as South Africa. You can be confident that we are able to manage your quality and information security with our ISO 9001 and ISO 27001 certifications.

iCompliance, a comprehensive digital platform, is designed to streamline Quality, Health, Safety, and Environment management, Environmental, Social, and Governance initiatives, and Governance, Risk, and Compliance processes for organizations in various industries. Our software provides tools for incident reporting and management, audit management, corrective action, and more. These tools help ensure compliance with regulations, standards, and safety, promote environmental responsibility, track ESG performances, engage stakeholders, manage regulatory requirements, internal control, and risk mitigation strategies, and ensure regulatory compliance. iCompliance's customizable workflows, real time analytics, integration options and mobile accessibility, as well as multilingual support, empower organizations to achieve operational excellence and mitigate risks.

CompliantPro Quality Management System Software ensures that a company's quality assurance needs are documented in one integrated system. This eliminates silos of information that can be managed as point solutions. CompliantPro allows organizations to manage their compliance and regulatory requirements beyond document control. The key areas are Environmental Health & Safety and Enterprise Risk Management, Training & Qualifications Audits, Customer / Supplier Management.

Web QMS, a cloud-based management software, helps you to achieve, maintain, and improve your ISO and API certifications. It also gives your employees full visibility to your quality and environmental management system. Web QMS modules and applications are designed to help you establish and maintain processes that conform to the API and ISO management system standards. You can have your entire management system under one roof with our many applications and modules.

Online document management makes it easy to create and manage documents. This prevents lost printed copies and a lack of organization. All information can be gathered in one place, making it easy to track and address any nonconformities. To aid you in decision making, define, collect and analyze KPIs using comparative charts. You can plan and execute actions to address opportunities and risks in a controlled and simple way. Get rid of spreadsheets and printed copies. Access file control in a cloud database with 24/7 access from any device and location. Optimize document review, approval, and elaboration. Manage access permissions, and receive automatic notifications about document changes or expiration dates. Genebra always has the most current version of any file that is uploaded. Don't waste time looking through multiple spreadsheets and don't lose any revisions.

Trusted by companies like Biogen, GE and Los Alamos DevonWay assists large businesses with quality management and work management. DevonWay helps businesses meet ISO 9001 standards. It also assists with minimizing risk, enhancing safety, and addressing any deficiencies.

qmsWrapper is an interconnected Quality Management Software for startups and small businesses. It helps all companies that want to increase productivity with ISO 9001:2015 and MedDev creators to easily achieve and manage ISO 13485:2016 and 21 CFR 820. Best For 1. For companies who need guidance to implement and adopt validated QMS. 2. For companies who want to automate their quality management and go beyond a paper-based system.

All templates can be formatted in Microsoft® Word or Excel, Publisher, Project, and are compatible with Microsoft(r] Office Versions 2000-2010. CASBuy offers quick solutions to Corporate Managers, Purchasing Professionals and Contract Administrators. All templates can be formatted in Microsoft® Word, Excel, Publisher or Project and are compatible with Microsoft® Office Versions 2000 - 2010. Our goal is to be the "One-Stop Shop" for professionals who need quick, basic information in a user-friendly format. When you consider how long it takes to complete a complex task from scratch, our prices are very reasonable and cost-effective. All our products are Microsoft Office (Word Excel, Access, Access, PowerPoint, and so on). They are based on Microsoft Office so that they can be easily integrated into your existing business systems.

isorobot is an intelligent business management software, connecting people, processes, technology, assets, and capital to your business goals. Using our experience to help you build efficient, scalable systems within your business. isorobot is a business performance management software which carries the solutions that aims at sustainable excellence in which innovation, quality, efficiency, and sustainability are the key elements. The solutions are categorized based on core business domains, organizational maturity for a steady start and scale approach. isorobot also has an enterprise version to go big from day one for matured businesses. The basis of the isorobot model consists of people, process, technology, assets, and capital domains of any organization. It consists of a universal framework of concepts, thus enabling organizations to share information in an effective way, irrespective of the different sectors, cultures, and life stages in which they are located. Organizations can thus take isorobot framework as a model as it consists of the best practice business excellence, governance, enterprise risk, compliance, process, strategy, internal audit frameworks, regulatory standards and guidelines.

ZipQuality, a software-enabled medical device service, helps companies bring new products to the market. Our collaboration platform allows agile teams to make rapid design changes while maintaining regulatory compliance. System (processes and tool) pre-configured; no need to change your quality system. The integrated system is able to handle rapid design iterations in product documentation. Your team will be guided by experienced consultants at every stage. Software tools that are fully featured, scalable, and built on the powerful ENOVIA platform. Our integrated system allows for rapid design changes, while keeping data and documentation in sync. All records are maintained in a audit-ready condition. Product requirements, Hardware requirements, Software requirements. We have a deep understanding of complex, software-intensive devices. ZipQuality is a structured documentation system that supports good systems engineering and efficient risk management. It also provides clear traceability.

Engage users from the front line to the C-suite with our configurable solutions--purpose-built with best-practice-based workflows and features--and embedded with AI, analytics, and mobile technology to quickly enhance performance at every stage of your digital transformation. Proven, flexible and powerful. Ready to deploy in three months or less. Organically built with, by, and for functional leader like you. Integrate with enterprise systems to deliver a superior user experience. Extend best-practice workflows, a versionless platform, and powerful pre-built configuration options with quick-to launch. Engage, communicate and drive key stakeholder performances via the industry's robust, integrated Mobile & Analytics platform.

All risk management activities should be recorded and readily accessible for inspection. Most healthcare leaders are aware that their accreditation legally and morally requires them to implement risk management. Many have not, as the law was not strictly enforced. The Omni-Assistant enterprise system is a modular, sophisticated system. It is intuitive, fully integrated and optimized to support best business practices. The Omni-Assistant Core, the dominant module, connects and successfully links all modules. The processes can be activated from one module into another using specific business rules, allowing seamless integration. The robust workflow engine design efficiently initiates and creates triggers and events based upon your business requirements.

Paradigm 3 is both a web- and desktop-based platform that helps businesses manage compliance in document control, CAPA compliance, Competency Tracking, Training, and Document Control. The software includes tools such as an event manager to handle customer complaints and incident investigations, as well as tasks sent by e-mail and audit preparations. Paradigm 3 is beneficial to the following industries: Manufacturing, Test Labs, Healthcare, and Service Industries.

One platform for compliance, risk management, governance. GRC gives you and your colleagues an overview and helps you to manage and document your compliance, risks management, and ongoing control. The process is simplified and everyone involved needs to know only one system. This increases efficiency. No matter what industry you work in, there are regulations and standards you must adhere to and documentation that proves it. It is a complex project for many. Complex legislations and many requirements make it difficult to get support from the rest. Compliance will not be easy. However, RISMA's solution may make compliance simple so you can focus on what you are good at.

AURA is a web-based QMS software that allows organizations to monitor and manage their quality compliance activities. We bring you organization-specific quality management system and enable you to streamline your quality process for better risk management and assured compliance. Aura audit management software allows you to maintain quality standards for different business areas within your enterprise.

CWA SmartProcess (Business Process Management) software is robust and can be used for workflow management, process management, quality management, and process management. This web-based solution allows for simple modeling, optimization, publication, and publication (of documents and processes) using one platform. CWA SmartProcess offers optional modules for measures and tasks, claims, complaints, audits, and audits. CWA Smart Process allows you to seamlessly automate workflows and make continuous improvements in your business.

icmInspector automates control, review, and audit processes. It includes a central component responsible for administration and management, and a mobile app for Android. Improvement of the quality of the organization through the use of modern inspection, control, and interial audit procedures that enable the detection of irregular or undesirable situations in a dispersed, real-time manner. By replacing paper versions with electronic versions, you can reduce operating costs and minimize time spent on material preparation and distribution. Tools that enable fast data collection, protect against omissions and offer the possibility of scheduling work can increase the efficiency of those who are responsible for audits and controls. Eliminate fraud, abuses, and errors in the control process by recording metadata about data collection and enforcing only logically permissible answers.

Digitize your processes. Security. Environment. Qualitative. Hygiene. Of Business. Centralize. Simplify. Automate. All your tasks can be managed with one tool. Your organization's sustainability and performance. Automated processes are the foundation of safety and performance. BlueKanGo is the digital EHSQ platform to manage them. BlueKanGo is the digital EHSQ solution that has been trusted by over 3500 customers for 18 years. Digitize your Quality, EHS, and other processes. Quality and audits management. Employee safety and health. Environment. CMMS & inspection. Certification, Standards. Corporate Social Responsibility (CSR). Regulatory Watch. Strategic Planning. 6 key differences that make BlueKanGo different. BlueKanGo has been around for 18 years and is the SaaS platform with no boundaries. BlueKanGo is an innovative, scalable, and all-inclusive solution

A compliance and risk management system is essential for many contracts. It can help you to build a strong and sustainable business and give you a competitive edge in the marketplace. Your system must be more efficient, better, and smarter in today's economic climate. Qudos is passionate about helping you achieve this. Qudos' IMS software, online resources library, training for auditors, and professional consulting services have helped hundreds to improve their management systems, attain certification, and maintain compliance. Contact us now by email or phone to discuss your compliance- and risk management system requirements. Qudos has both the software and the expertise to help you implement and manage your compliance and risk management system more efficiently, better and smarter.

We have created simple and effective tools that will help you manage your EDM as well as the validation of your documents. Clear dashboards, customized forms, and real-time indicators allow you to track your workflow precisely. Qualios combines two powerful tools to help you manage your workflow. Qualios Doc allows you to manage your documents and their evolution, ensuring that up-to-date information is always available. Qualios Manager can be customized to suit your quality indicators. To manage your internal workflow, create clear and concise forms and dashboards. You need to be able to quickly control all your flows in order to improve your process. Qualios was designed to support your quality commitment and allow you to comply with ISO 9001 or ISO 14001 standards. These improvements should not be tedious or time-consuming

Each organization structure is unique and requires a customized approach to address concerns regarding international standards. This is often a time-consuming process. ISMS Solutions has developed Conformance Works, a proprietary platform that guides customers through an automated process to help them comply with any ISO standard. Conformance Works simplifies and personalizes each organization's standard certification process. A built-in document management system, global editor, compliance management system and risk assessment module make company documentation easy and efficient. Software will be available via multiple digital means. This allows for faster implementation of ISO standards to certification. It simplifies the process of meeting or exceeding ISO standards.

Limsophy BPM is for quality management requirements. A lean quality management system with clear document handling is the best way to ensure a consistent high quality product with acceptable effort. Limsophy provides support for creating and managing QM documents. It also gives access to other management functions like audit planning, risk management, target management, and the continuous improvement process. Limsophy BPM (Business Process Management) is the standard information management system for managing business process (Business Process Management). Over 10,000 people use our QM software every day. It is used in all industries. Users can access their documents and processes via the browser. They can also capture valuable inputs to the QM software. Because all links are generated from the same database, they work. Process management in Limsophy BPM ensures consistency in flow charts, process documents and tools.

SoftExpert EQM (enterprise quality management software) is the most comprehensive. It assists companies in achieving and maintaining ISO 9001 certification by automating highly interactive quality processes that are tailored to their specific products, operations, and business practices. As a modular and scalable solution platform, SoftExpert Quality Management Software seamlessly integrates all key quality initiatives, including process mapping, documented information (SOP - standard operating procedures, work instructions and records), non-conformance reports (NCR/NCMR), corrective/preventive actions (CAPA), quality indicators (KPIs). The solution can also manage supplier relations, customer complaints and quality audits, as well as competence and training, quality controls, quality inspection, and statistical process control, increasing QMS flexibility and robustness.

QMSrs is the central hub for automated quality and business excellence solutions that enhance business performance. We deliver confidence in quality. Our modular automated products can be used to support any type of organization, including multi-site or multi-national operations. Modules can be added to the business as it grows or as budgets permit. QMSrs automated solutions can be used to support any type of organization, including multi-site or multi-national operations. QMSrs solutions offer robust capabilities for workflow management, document administration, electronic delivery of alerts, notifications, and real time reporting and analysis. We are experts in Quality Excellence Solutions. Risk management is the ability to manage uncertainty and its effects on an organization in order to prevent it from happening again. Our Risk Management Solutions can help organizations reduce the cost of any risk.